Silver halide color photographic light-sensitive material

ABSTRACT

A silver halide color photographic light-sensitive material, having at least one each of blue-, green-, and red-sensitive emulsion layers containing yellow, magenta, and cyan couplers, respectively, on a support; wherein said blue-sensitive emulsion layer contains at least one coupler of formula (I); and 
 
wherein the light-sensitive material satisfies expression a-1) and/or b-1):  
                 
wherein, Q forms a 5- to 7-membered ring with the —N═C—N(R1)-; R1 and R2 each are a substituent; m is 0 to 5; and X is a hydrogen atom, or a coupling split-off group; 
 
0.5≦ D max( UV )/ D min( UV )≦1.1  a-1) 
wherein Dmax(UV)/Dmin(UV) is the smallest of the value in a wavelength range of 340 to 450 nm; 
 
1300≦( B−C )/ A ≦20000  b-1) 
         wherein B is yellow Dmax, C is yellow Dmin; and A is an amount mol/m 2  of the coupler of formula (I).

CROSS-REFERENCE TO RELATED APPLICATION

This application is a Divisional of U.S. application Ser. No. 11/594,782filed Nov. 9, 2006, which is a divisional of U.S. application Ser. No.10/969,205 filed Oct. 21, 2004, issued as U.S. Pat. No. 7,183,044, whichis a continuation of U.S. application Ser. No. 10/375,053 filed Feb. 28,2003, abandoned; the above-noted applications incorporated herein byreference in their entirety.

FIELD OF THE INVENTION

The present invention relates to a silver halide photographiclight-sensitive material, and, particularly, to a photographiclight-sensitive material which attains improvement on the property forpreventing static-induced fog from occurring without deterioratingproperties for photographic light-sensitive materials, typified bysharpness, processability, and the like.

Further, the present invention relates to a silver halide colorphotographic light-sensitive material, and particularly to a silverhalide color photographic light-sensitive material which is excellent incolor reproducibility and rapid processability.

Further, the present invention relates to a silver halide colorphotographic light-sensitive material which is excellent in rapidprocessability, color reproducibility, preserving stability thereof inan unexposed state, and image fastness after processing.

Further, the present invention relates to a silver halide colorphotographic light-sensitive material with an increased silver andcoupler utilization efficiency, allowing reduction in the coating amountof a material, having excellent suitability to a rapid high-productivityprocessing and cost reduction capability. The present invention alsorelates to a method for forming an image by using the silver halidecolor photographic light-sensitive material.

More particularly, the present invention relates to a silver halidecolor photographic light-sensitive material with which the period forforming an image by color development, the period for bleach fixing, andthe period for washing with water can be shortened without exerting aharmful effect; and to a method for forming an image by using the same.

BACKGROUND OF THE INVENTION

In a silver halide photographic light-sensitive material (hereinafter,sometimes referred to simply as “a light-sensitive material”) forsubtractive color photography, a color image is formed by dyes of threeprimary colors of yellow, magenta, and cyan. In the color photographythat uses a current p-phenylenediamine-series color-developing agent, anacylacetoanilide-series compound is used as a yellow coupler. However,the hue of the yellow dyes obtained from these yellow couplers becomesreddish, due to an inferior sharpness of a peak of the absorption curveat the longer wavelength side (that is, on the absorption curve, thepeak in interest has subsidiary absorption at its foot portion at thelonger wavelength side), which renders it difficult to obtain a yellowhue with high purity. Further, because the molecular extinctioncoefficient of the yellow dyes is low, it is necessary, to attain adesired color density, to use larger amounts of both of the coupler andthe silver halide. The use of such larger amounts of these componentsraises the problem that the resulting increase in thickness of alight-sensitive material sometimes lowers the sharpness of the obtainedcolor image. Further, accompanying sensitivity enhancement of a colorphotosensitive material in recent years, static-induced fog often occursat the time of shooting with or producing of the color photosensitivematerial. Therefore, it has been desired to solve the problem.

In order to solve such the problems, improvement of acyl groups andanilido groups were proposed on the couplers. Recently, as improvedcouplers of the conventional acylacetoanilide-series, there wereproposed, for example, 1-alkylcyclopropanecarbonyl acetoanilide-seriescompounds, described in JP-A-4-218042 (“JP-A” means unexamined publishedJapanese patent application); cyclomalonic acid diamide-type couplers,described in JP-A-5-11416; pyrrole-2- or 3-yl- or indole-2- or3-yl-carbonylacetoanilide-series couplers, described in, for example,European Patent Nos. 953870A1, 953871A1, 953872A1, 953873A1, 953874A1and 953875A1. The dyes formed from these couplers were improved in termsof both of hue and molecular extinction coefficient of dyes formed,compared with the conventional ones. However, they are not satisfactoryin image stability still. Further, owing to their complicated chemicalstructure, the synthesis route became longer, and consequently cost ofthe couplers became higher, causing a practical problem. In addition,U.S. Pat. No. 3,841,880, JP-A-52-82423 and JP-A-2-28645 propose acetateester-series and acetoanilide-series couplers to which1,2,4-benzothiadiazine-1,1-dioxide is bonded. However, these couplersare low in color-forming property, and they are inferior in sharpness ofa peak of the absorption curve owing to the foot portion on the longerwavelength side. Therefore, improvement of these properties has beendesired. As a preventive measure for static-induced fog, it is known,for example, to add an ultraviolet-ray absorber (UV agent) to aprotecting layer of a light-sensitive material, as described inJP-A-6-130549. However, when an amount of the UV agent to be used isincreased for the purpose for further improving a property forpreventing static-induced fog, the film thickness of the resultinglight-sensitive material becomes to be thick, to cause deterioration ofsharpness of an image and (rapid) processability, which is notpreferable.

Silver halide photographic light-sensitive materials have been widelyused until today as materials that are inexpensive, have stable quality,and provide an image with high quality. However, there is an increaseddemand by users for image quality enhancement, enhancement in stabilityof quality, and enhancement in productivity. As to the demand for imagequality enhancement, improvements in whiteness, color reproducibility,and sharpness are demanded. As to the demand for enhancement instability of quality, it is required to improve stability in theproduction of a light-sensitive material, stability during storage withthe lapse of time in an unexposed state, and performance stabilityduring development processing. Also, as to improving productivity,processing speed enhancement is strongly required.

Particularly, color reproducibility is important for photographiclight-sensitive materials, such as color papers and color reversals,used for direct appreciation. To improve color reproducibility, first,it is necessary for the dye formed by a coupling reaction between adye-forming coupler (hereinafter also referred to simply as a coupler)and an oxidized product of a developing agent, to itself be reduced inunnecessary absorption and have good absorbing characteristics. Further,in addition to the above, it is also important for, for example,remaining color due to a sensitizing dye, an irradiation-preventing dye,or the like, to be less, and fogging to be less.

To sufficiently exhibit color reproducibility of the formed dye, it isimportant for a light-sensitive material to be stable during developmentprocessing. Also, to sufficiently exhibit color reproducibility of theformed dye, it is important for 1) the change in performance of alight-sensitive material during storage in an unexposed state, to besmall, and 2) a light-sensitive material to be stable during developmentprocessing. Also, if a dye image after processing is stable, ahigh-quality photographic image can be stored for a long period of time.

Particularly, technologies for the purpose to attain a reduction in theamount of a silver halide emulsion in a silver halide color photographiclight-sensitive material, and to form a thin layer of a light-sensitivematerial, are demanded, from the viewpoint of improving productivity.

In recent years, in the field of photographic processing services, aphotographic light-sensitive material that can be processed rapidly andform a high-quality image is demanded as part of improvement of serviceto users and as means for improving productivity. To respond to thisdemand, currently, a rapid processing is usually carried out in which aphotographic light-sensitive material containing a high silver chlorideemulsion (hereinafter, also referred to as “high silver chlorideprinting material”) is processed in 45 seconds for a color developingtime, and in about 4 minutes for a total processing time of from thestart of the developing step to the completion of the drying step (forexample, Color Processing CP-48S (trade name) or the like, manufacturedby Fuji Photo Film Co., Ltd.). However, as compared with the rapidity ofmaking images by other color image making methods (for example, anelectrostatic transfer method, a thermal transfer method, an ink jetmethod), it cannot be said that even this rapid development processingsystem for high silver chloride printing materials provides asatisfactory rapidity. For this reason, there are demands for asuper-rapid processing, of which the total processing time from thestart of development of and the completion of drying of a high silverchloride color printing material, is on the level of below 1 minute.

Therefore, in the art of this field, various studies on means to improvesuper-rapid processing suitability and efforts for achieving it havebeen made. For example, as means for improving super-rapid processingsuitability,

(1) reduction in the coating amount of an organic material by adoptionof a highly active coupler and a coupler giving a high molecularextinction coefficient of a coloring dye, and reduction in the coatingamount of a hydrophilic binder, (2) adoption of a silver halide emulsionhaving a high development speed, and the like, have been studied. Also,a method for increasing the development speed by coating a silver halideemulsion layer having the lowest color-development speed (correspondingto the yellow coupler-containing layer in conventional color printingmaterials) on a more distant side from the support than other silverhalide emulsion layers containing other couplers, has been known. Thismethod has been proposed in, for example, JP-A-7-239538 andJP-A-7-239539.

Further, a method for enhancing a development speed, in which theposition of a yellow coupler-containing layer is set on a relativelydistant side from the support than at least one of a silver halideemulsion layer containing a magenta coupler and a silver halide emulsionlayer containing a cyan coupler in order to make the developing agenteasily permeate through the layer containing a yellow coupler that has alow color-developing speed, and, in addition, in which the amount of ahydrophilic binder is reduced, has been proposed in JP-A-2000-284428.However, locating the layer containing a yellow coupler upper than atleast one of the layer containing a magenta coupler and the layercontaining a cyan coupler without taking into consideration the balanceamong the coupling activities in the color forming layers, results inthat the coupler coupling fails to win the competition with thecolor-mixing preventing layer, so that an oxidized product of acolor-developing agent is lost. Actually, silver saving on the ultimatelevel has not been achieved yet. Use of thinner layers for rapidprocessing by reducing the amount of binder without taking intoconsideration the balance between the utilization efficiency of anoxidized product of a color-developing agent and the coupling activity,lowers the protective colloid function of the binder, and causes failurein image storability such as causing blurring of a color image.

Furthermore, according to JP-A-2-298936, the relative coupling rate of ayellow coupler and the dielectric constant of oil droplets arecontrolled by coemulsifying the yellow coupler with a cyan coupler.However, increasing the activity of the yellow coupler alone isundesirable in view of the balance, and has disadvantages in that thecolor mixing preventing layer must be thicker than ever, stain tends tooccur due to the developing agent, and the like. Also, in the techniquein which the relative coupling activity is controlled, co-emulsificationresults in an increase in the volume of oil droplets, which varies theamount of the developing agent incorporated, so that in some cases, theactivity cannot be estimated exactly.

Also, in JP-A-5-303182, proposed is a method in which apyrrolotriazole-type cyan coupler is applied to arrange between acolor-forming layer containing a yellow coupler and a color-forminglayer containing a magenta coupler, from the viewpoint of balance ofcoupling activities. However, the intention of the present invention isnot satisfied by this method, because the amount of oil soluble contentsin a high-boiling organic solvent dispersing therein thepyrrolotriazole-type cyan coupler is small and the activity in the oildroplets is low.

SUMMARY OF THE INVENTION

The present invention is a silver halide color photographiclight-sensitive material, which has at least one blue-sensitive emulsionlayer containing a yellow coupler, at least one green-sensitive emulsionlayer containing a magenta coupler, and at least one red-sensitiveemulsion layer containing a cyan coupler, on a support;wherein said blue-sensitive emulsion layer contains at least one couplerrepresented by formula (I); and wherein the silver halide colorphotographic light-sensitive material satisfies the following expressiona-1) and/or b-1):

wherein, in formula (I), Q represents a group of non-metal atomsnecessary to form a 5- to 7-membered ring together with the —N═C—N(R1)-;R1 represents a substituent; R2 represents a substituent; m represents 0(zero) or an integer of 1 to 5; when m is 2 or more, R2s may be the sameor different from each other, or R2s may bond together to form a ring;and X represents a hydrogen atom, or a group capable of being split-offupon a coupling reaction with an oxidized product of a developing agent;0.5≦Dmax(UV)/Dmin(UV)≦1.1  a-1)

wherein Dmax(UV)/Dmin(UV) is the smallest value in a range of wavelengthUV, in which UV is a wavelength within the range of 340 nm or more and450 nm or less, among values represented by (an absorbance at awavelength UV, for a portion having the yellow maximum colordensity)/(an absorbance at the wavelength UV, for a portion having theyellow minimum color density);11300≦(B−C)/A≦20000  b-1)

wherein B represents the maximum color density of yellow, C representsthe minimum color density of yellow, each of which means a transmissiondensity when the support is a transmissive support, or a reflectiondensity when the support is a reflective support; and A is an amountmol/m² of the coupler represented by formula (I) to be used.

Further, the present invention is a silver halide color photographiclight-sensitive material, which has at least one yellow color-forminglight-sensitive silver halide emulsion layer, at least one magentacolor-forming light-sensitive silver halide emulsion layer, and at leastone cyan color-forming light-sensitive silver halide emulsion layer, ona support, andwhich contains at least one yellow dye-forming coupler represented bythe above formula (I) and at least one cyan coupler represented by thefollowing formula (CC-I):

wherein, in formula (CC-I), G_(a) represents —C(R₂₃)=or —N═; G_(b)represents —C(R₂₃)=when G_(a) represents —N═, or G_(b) represents—N=when G_(a) represents —C(R₂₃)=; R₂₁, and R₂₂ each independentlyrepresent an electron attractive group of which a Hammett's substituentconstant σ_(p) value is 0.20 or more and 1.0 or less; R₂₃ represents asubstituent; and Y represents a hydrogen atom, or a group capable ofbeing split-off upon a coupling reaction with an oxidized product of adeveloping agent.

Further, the present invention is a silver halide color photographiclight-sensitive material, which has at least one yellow color-forminglight-sensitive silver halide emulsion layer, at least one magentacolor-forming light-sensitive silver halide emulsion layer, and at leastone cyan color-forming light-sensitive silver halide emulsion layer, ona support, andwhich contains at least one yellow dye-forming coupler represented bythe above formula (I), and at least one compound selected from the groupconsisting of compounds represented by any of the following formula[S-I], [S-II], [S-III], [S-IV], [S-V], [S-VI], [ST-I], [ST-II],[ST-III], [ST-IV] or [ST-V] and water-insoluble homopolymers orcopolymers:

wherein, in formula [S-I], R_(s1), R_(s2) and R_(s3) each independentlyrepresent an alkyl group, a cycloalkyl group, an alkenyl group or anaryl group, in which the total number of carbon atoms contained in thegroups represented by R_(s1), R_(s2) and R_(s3) is 12 to 60;

wherein, in formula [S-II], R_(s4) and R_(s5) each independentlyrepresent an alkyl group, a cycloalkyl group, an alkoxy group or ahalogen atom; s1 represents an integer from 0 to 4; and when s1 is 2 ormore, plural R_(s5)s may be the same or different, and R_(s4) and R_(s5)may bond with each other to form a five- or six-membered ring;R_(s6)-(-COOR_(s7))  formula [S-III]

wherein, in formula [S-III], R_(s6) represents a linking group having noaromatic group; R_(s7) represents an alkyl, cycloalkyl, alkenyl oralkynyl group having 20 or less carbon atoms; sm represents an integerfrom 2 or more and 5 or less; and when sm is 2 or more, plural—COOR_(s7)s may be the same or different;R_(s5)-(-OCOR_(s9))_(sn)  formula [S-IV]

wherein, in formula [S-IV], R_(s8) represents a linking group; R_(s9)represents an alkyl, cycloalkyl, alkenyl or alkynyl group having 20 orless carbon atoms; sn represents an integer from 2 or more and 5 orless; and when sn is 2 or more, plural —OCOR_(s9)s may be the same ordifferent;

wherein, in formula [S-V], R_(s10), R_(s11), R_(s12) and R_(s13) eachindependently represent a hydrogen atom, an aliphatic group, analiphatic oxycarbonyl group, an aromatic oxycarbonyl group or acarbamoyl group, in which the total number of carbon atoms contained inR_(s10), R_(s11), R_(s11) and R_(s13) is 8 to 60; and R_(s10) andR_(s11), R_(s10) and R_(s12), or R_(s12) and R_(s13) may bond with eachother, to form a five- to seven-membered ring, respectively; with theproviso that all of R_(s10), R_(s11), R_(s12) and R_(s13) simultaneouslydo not represent a hydrogen atom;R_(s14)-(-COOR_(s15))_(sp)  formula [S-VI]

wherein, in formula [S-VI], R_(s14) represents an aromatic linkinggroup; R_(s15) represents an alkyl, cycloalkyl, alkenyl or alkynyl grouphaving 20 or less carbon atoms; sp represents an integer from 3 or moreand 5 or less; and when sp is 2 or more, plural —COOR_(s15)s may be thesame or different;

wherein, in formula [ST-I], R₄₀, R₅₀ and R₆₀ each independentlyrepresent an aliphatic group or an aromatic group; and 14, m4 and n4each independently represent 0 or 1, with the proviso that 14, m4 and n4simultaneously are not 1;R_(A)—NH—SO₂—R_(B)  formula [ST-II]

wherein, in formula [ST-II], R_(A) and R_(B) each independentlyrepresent a hydrogen atom, an alkyl group, a cycloalkyl group, analkenyl group, a cycloalkenyl group, an alkynyl group, an aryl group, aheterocyclic group, an alkoxy group, an aryloxy group, a heterocyclicoxy group, or a group represented by the following formula:

in which R_(C) and R_(D) each independently represent a hydrogen atom,an alkyl group or an aryl group; and R_(A) and R_(B) each may be thesame or different;

wherein, in formula [ST-III], J′ represents a divalent organic group;and Y represents an alkyl group, a cycloalkyl group, an aryl group, analkenyl group, an alkynyl group, a cycloalkenyl group or a heterocyclicgroup;

wherein, in formula [ST-IV], R₅₁ and R₅₂ each independently represent analiphatic group or —COR₅₃, in which R₅₃ represents an aliphatic group;J₅ represents a divalent organic group or simply a connecting bond; andl₅ represents an integer from 0 to 6; andR₅₄—Y₅₄  formula [ST-V]

wherein, in formula [ST-V], R₅₄ represents a hydrophobic group havingthe total number of carbon atoms of 10 or more; and Y₅₄ represents amonovalent organic group containing an alcoholic hydroxyl group.

Further, the present invention is a silver halide color photographiclight-sensitive material, which has, on a support, at least one yellowcolor-forming light-sensitive silver halide emulsion layer, at least onemagenta color-forming light-sensitive silver halide emulsion layer, andat least one cyan color-forming light-sensitive silver halide emulsionlayer, and which has at least one non-light-sensitive andnon-color-forming hydrophilic colloid layer,

wherein the silver halide color photographic light-sensitive materialcomprises a high silver chloride emulsion containing silver halidegrains with a silver chloride content of 95 mol % or more, and

wherein a color-forming coupler contained in the color-forminglight-sensitive silver halide emulsion layers has an average relativecoupling rate, kar, to a compound A of the following formula, of 0.6 ormore and 2.0 or less.

Other and further features and advantages of the invention will appearmore fully from the following description.

DETAILED DESCRIPTION OF THE INVENTION

According to the present invention, there is provided the followingmeans:

(1) A silver halide color photographic light-sensitive material, havingat least one blue-sensitive emulsion layer containing a yellow coupler,at least one green-sensitive emulsion layer containing a magentacoupler, and at least one red-sensitive emulsion layer containing a cyancoupler, on a support;

wherein said blue-sensitive emulsion layer contains at least one couplerrepresented by formula (I); and

wherein the silver halide color photographic light-sensitive materialsatisfies the following expression a-1) and/or b-1):

wherein, in formula (I), Q represents a group of non-metal atomsnecessary to form a 5- to 7-membered ring together with the —N—C—N(R1)-;R1 represents a substituent; R2 represents a substituent; m represents 0(zero) or an integer of 1 to 5; when m is 2 or more, R_(2s) may be thesame or different from each other, or R2s may bond together to form aring; and X represents a hydrogen atom, or a group capable of beingsplit-off upon a coupling reaction with an oxidized product of adeveloping agent;0.5≦Dmax(UV)/Dmin(UV)≦1.1  a-1)

wherein Dmax(UV)/Dmin(UV) is the smallest value in a range of wavelengthUV, in which UV is a wavelength within the range of 340 nm or more and450 nm or less, among values represented by (an absorbance at awavelength UV, for a portion having the yellow maximum colordensity)/(an absorbance at the wavelength UV, for a portion having theyellow minimum color density);1300≦(B−C)/A≦20000  b-1)

wherein B represents the maximum color density of yellow, C representsthe minimum color density of yellow, each of which means a transmissiondensity when the support is a transmissive support, or a reflectiondensity when the support is a reflective support; and A is an amountmol/m of the coupler represented by formula (I) to be used.

(2) The silver halide color photographic light-sensitive materialaccording to the above item (1), wherein Q in the above-mentionedformula (I) is a group represented by —C(—R11)=C(—R12)—SO₂— or—C(—R11)=C(—R12)—CO—, in which R11 and R12 bond with each other to forma 5- to 7-membered ring together with the —C═C—, or R11 and R12 eachindependently represent a hydrogen atom or a substituent.(3) The silver halide color photographic light-sensitive materialaccording to the above item (1), wherein the coupler represented byformula (I) is a coupler represented by formula (II):

wherein, in formula (II), R1, R2, m and X each have the same meanings asthose in formula (I); R3 represents a substituent; n represents 0 (zero)or an integer of 1 to 4; when n is 2 or more, R3s may be the same ordifferent, or R3s may bond together to form a ring.

(4) The silver halide color photographic light-sensitive materialaccording to any one of the above items (1) to (3), wherein the supportis a transmissive support, and wherein the silver halide colorphotographic light-sensitive material satisfies the following expressiona-2):0.5≦Dmax(UV)/Dmin(UV)≦0.9  a-2)(5) The silver halide color photographic light-sensitive materialaccording to any one of the above items (1) to (3), wherein the supportis a transmissive support, and wherein the silver halide colorphotographic light-sensitive material satisfies the following expressiona-2) and/or b-2):0.5≦Dmax(UV)/Dmin(UV)≦0.9  a-2)1700≦(B−C)/A≦10000  b-2)(6) The silver halide color photographic light-sensitive materialaccording to any one of the above items (1) to (3), wherein the supportis a reflective support, and wherein the silver halide colorphotographic light-sensitive material satisfies the following expressiona-1) and/or b-3):0.5≦Dmax(UV)/Dmin(UV)≦1.1  a-1)4200≦(B−C)/A≦20000  b-3)(7) The silver halide color photographic light-sensitive materialaccording to any one of the above items (1) to (6), having at least oneemulsion layer containing a silver halide emulsion that contains silverhalide grains whose silver chloride content is 95 mole % or more.(8) A method of forming a color-image, comprising the steps of:

exposing image-wise the silver halide color photographic light-sensitivematerial as described in any one of the above items (1), (2), (3), (4),(5) or (7);

subjecting the exposed silver halide color photographic light-sensitivematerial to black-and white development;

subjecting the silver halide color photographic light-sensitive materialto reversal-processing; and

subjecting the silver halide color photographic light-sensitive materialto color development.

(Hereinafter, a first embodiment of the present invention means toinclude the silver halide color photographic light-sensitive materialsor the method of forming a color image, as described in the items (1) to(8) above.)

(9) A silver halide color photographic light-sensitive material, havingat least one yellow color-forming light-sensitive silver halide emulsionlayer, at least one magenta color-forming light-sensitive silver halideemulsion layer, and at least one cyan color-forming light-sensitivesilver halide emulsion layer, on a support, and

containing at least one yellow dye-forming coupler represented by thefollowing formula (I) and at least one cyan coupler represented by thefollowing formula (CC-I):

wherein, in formula (I), Q represents a group of non-metal atomsnecessary to form a 5- to 7-membered ring together with the —N═C—N(R1)—;R1 represents a substituent; R2 represents a substituent; m representsan integer of 0 to 5; when m is 2 or more, R2s may be the same ordifferent from each other, or R2s may bond together to form a ring; andX represents a hydrogen atom, or a group capable of being split-off upona coupling reaction with an oxidized product of a developing agent;

wherein, in formula (CC-I), G_(a) represents —C(R₂₃)═ or —N═; G_(b)represents —C(R₂₃)=when G_(a) represents —N═, or G_(b) represents—N=when G_(a) represents —C(R₂₃)═; R₂₁ and R₂₂ each independentlyrepresent an electron attractive group of which a Hammett's substituentconstant σ_(p) value is 0.20 or more and 1.0 or less; R₂₃ represents asubstituent; and Y represents a hydrogen atom, or a group capable ofbeing split-off upon a coupling reaction with an oxidized product of adeveloping agent.

(10) The silver halide color photographic light-sensitive materialaccording to the above item (9), wherein Q in the above-mentionedformula (I) is a group represented by —C(—R11)=C(—R12)—SO₂— or—C(—R11)=C(—R12)—CO—, in which R11 and R12 bond with each other to forma 5- to 7-membered ring together with the —C═C—, or R11 and R12 eachindependently represent a hydrogen atom or a substituent.

(11) The silver halide color-photographic light-sensitive materialaccording to the above item (9), wherein Q in the above-mentionedformula (I) is a group represented by —C(—R11)=C(—R12)—SO₂—, in whichR11 and R12 bond with each other to form a 5- to 7-membered ringtogether with the —C═C—, or R11 and R12 each independently represent ahydrogen atom or a substituent.(12) The silver halide color photographic light-sensitive materialaccording to the above item (9), wherein the yellow dye-forming couplerrepresented by formula (I) is a yellow dye-forming coupler representedby formula (II):

wherein, in formula (II), R1 represents a substituent; R2 represents asubstituent; m represents an integer of 0 to 5; when m is 2 or more, R2smay be the same or different from each other, or R2s may bond togetherto form a ring; R3 represents a substituent; n represents an integer of0 to 4; when n is 2 or more, R3s may be the same or different from eachother, or R3s may bond together to form a ring; and X represents ahydrogen atom, or a group capable of being split-off upon a couplingreaction with an oxidized product of a developing agent.

(13) The silver halide color photographic light-sensitive materialaccording to the above item (12), wherein R1 in the dye-forming couplerrepresented by formula (II) is a substituted or unsubstituted alkylgroup.

(Hereinafter, a second embodiment of the present invention means toinclude the silver halide color photographic light-sensitive materialsdescribed in the items (9) to (13) above.)

(14) A silver halide color photographic light-sensitive material, havingat least one yellow color-forming light-sensitive silver halide emulsionlayer, at least one magenta color-forming light-sensitive silver halideemulsion layer, and at least one cyan color-forming light-sensitivesilver halide emulsion layer, on a support, and

containing at least one yellow dye-forming coupler represented by thefollowing formula (I), and at least one compound selected from the groupconsisting of compounds represented by any of the following formula[S-I], [S-II], [S-III], [S-IV], [S-V], [S-VI], [ST-I], [ST-II],[ST-III], [ST-IV] or [ST-V] and water-insoluble homopolymers orcopolymers:

wherein, in formula (I), Q represents a group of non-metal atomsnecessary to form a 5- to 7-membered ring together with the —N═C—N(R1)—;R1 represents a substituent; R2 represents a substituent; m representsan integer of 0 to 5; when m is 2 or more, R2s may be the same ordifferent from each other, or R2s may bond together to form a ring; andX represents a hydrogen atom, or a group capable of being split-off upona coupling reaction with an oxidized product of a developing agent;

wherein, in formula [S-I], R_(s1), R_(s2) and R_(s3) each independentlyrepresent an alkyl group, a cycloalkyl group, an alkenyl group or anaryl group, in which the total number of carbon atoms contained in thegroups represented by R_(s1), R_(s2) and R_(s3) is 12 to 60;

wherein, in formula [S-II], R_(s4) and R_(s5) each independentlyrepresent an alkyl group, a cycloalkyl group, an alkoxy group or ahalogen atom; s1 represents an integer from 0 to 4; and when s1 is 2 ormore, plural R_(s5)s may be the same or different, and R_(s4) and R_(s5)may bond with each other to form a five- or six-membered ring;R_(s6)-(-COOR_(s7))_(sm)  formula [S-III]

wherein, in formula [S-III], R_(s6) represents a linking group having noaromatic group; R_(s7) represents an alkyl, cycloalkyl, alkenyl oralkynyl group having 20 or less carbon atoms; sm represents an integerfrom 2 or more and 5 or less; and when sm is 2 or more, plural—COOR_(17s) may be the same or different;R_(s8)-(-OCOR_(s9))_(sn)  formula [S-IV]

wherein, in formula [S-IV], R_(s8) represents a linking group; R_(s9)represents an alkyl, cycloalkyl, alkenyl or alkynyl group having 20 orless carbon atoms; sn represents an integer from 2 or more and 5 orless; and when sn is 2 or more, plural —OCOR_(s9)s may be the same ordifferent;

wherein, in formula [S-V], R_(s10), R_(s11), R_(s12) and R_(s13) eachindependently represent a hydrogen atom, an aliphatic group, analiphatic oxycarbonyl group, an aromatic oxycarbonyl group or acarbamoyl group, in which the total number of carbon atoms contained inR_(s10), R_(s11), R_(s12) and R_(s13) is 8 to 60; and R_(s10) andR_(s11), R_(s10) and R_(s12), or R_(s12) and R_(s13) may bond with eachother, to form a five- to seven-membered ring, respectively; with theproviso that all of R_(s10), R_(s11), R_(s12) and R_(s13) simultaneouslydo not represent a hydrogen atom;R_(s14)-(-COOR_(s15))_(sp)  formula [S-VI]

wherein, in formula [S-VI], R_(s14) represents an aromatic linkinggroup; R_(s15) represents an alkyl, cycloalkyl, alkenyl or alkynyl grouphaving 20 or less carbon atoms; sp represents an integer from 3 or moreand 5 or less; and when sp is 2 or more, plural —COOR_(s15)s may be thesame or different;

wherein, in formula [ST-I], R₄₀, R₅₀ and R₆₀ each independentlyrepresent an aliphatic group or an aromatic group; and 14, m4 and n4each independently represent 0 or 1, with the proviso that 14, m4 and n4simultaneously are not 1;R_(A)—NH—SO₂—R_(B)  formula [ST-II]

wherein, in formula [ST-II], R_(A) and R_(B) each independentlyrepresent a hydrogen atom, an alkyl group, a cycloalkyl group, analkenyl group, a cycloalkenyl group, an alkynyl group, an aryl group, aheterocyclic group, an alkoxy group, an aryloxy group, a heterocyclicoxy group, or a group represented by the following formula:

in which R_(C) and R_(D) each independently represent a hydrogen atom,an alkyl group or an aryl group; and R_(A) and R_(B) each may be thesame or different;

wherein, in formula [ST-III], J′ represents a divalent organic group;and Y represents an alkyl group, a cycloalkyl group, an aryl group, analkenyl group, an alkynyl group, a cycloalkenyl group or a heterocyclicgroup;

wherein, in formula [ST-IV], R₅₁ and R₅₂ each independently represent analiphatic group or —COR₅₃, in which R₅₃ represents an aliphatic group;J₅ represents a divalent organic group or simply a connecting bond; andl₅ represents an integer from 0 to 6; andR₅₄—Y₅₄  formula [ST-V]

wherein, in formula [ST-V], R₅₄ represents a hydrophobic group havingthe total number of carbon atoms of 10 or more; and Y₅₄ represents amonovalent organic group containing an alcoholic hydroxyl group.

(15) The silver halide color photographic light-sensitive materialaccording to the above item (14), wherein Q in the above-mentionedformula (I) is a group represented by —C(—R11)=C(—R12)—SO₂— or—C(—R11)=C(—R12)—CO—, in which R11 and R12 bond with each other to forma 5- to 7-membered ring together with the —C═C—, or R11 and R12 eachindependently represent a hydrogen atom or a substituent.

(16) The silver halide color photographic light-sensitive materialaccording to the above item (14), wherein Q in the above-mentionedformula (I) is a group represented by —C(—R11)=C(—R12)—SO₂—, in whichR11 and R12 bond with each other to form a 5- to 7-membered ringtogether with the —C═C—, or R11 and R12 each independently represent ahydrogen atom or a substituent.(17) The silver halide color photographic light-sensitive materialaccording to the above item (14), wherein the yellow dye-forming couplerrepresented by formula (I) is a yellow dye-forming coupler representedby formula (II):

wherein, in formula (II), R1 represents a substituent; R2 represents asubstituent; m represents an integer of 0 to 5; when m is 2 or more, R2smay be the same or different from each other, or R2s may bond togetherto form a ring; R3 represents a substituent; n represents an integer of0 to 4; when n is 2 or more, R3s may be the same or different from eachother, or R3s may bond together to form a ring; and X represents ahydrogen atom, or a group capable of being split-off upon a couplingreaction with an oxidized product of a developing agent.

(18) The silver halide color photographic light-sensitive materialaccording to the above item (17), wherein R1 in the dye-forming couplerrepresented by formula (II) is a substituted or unsubstituted alkylgroup.

(Hereinafter, a third embodiment of the present invention means toinclude the silver halide color photographic light-sensitive materialsdescribed in the items (14) to (18) above.)

(19) A silver halide color photographic light-sensitive material,having, on a support, at least one yellow color-forming light-sensitivesilver halide emulsion layer, at least one magenta color-forminglight-sensitive silver halide emulsion layer, and at least one cyancolor-forming light-sensitive silver halide emulsion layer, and havingat least one non-light-sensitive and non-color-forming hydrophiliccolloid layer,

wherein the silver halide color photographic light-sensitive materialcomprises a high silver chloride emulsion containing silver halidegrains with a silver chloride content of 95 mol % or more, and

wherein a color-forming coupler contained in the color-forminglight-sensitive silver halide emulsion layers has an average relativecoupling rate, kar, to a compound A of the following formula, of 0.6 ormore and 2.0 or less.

(20) The silver halide color photographic light-sensitive materialaccording to the item (19) above, wherein the color-forminglight-sensitive silver halide emulsion layer containing thecolor-forming coupler that has the maximum value of the average relativecoupling rate, kar, is provided as an intermediate layer among the threecolor of cyan, magenta and yellow color-forming light-sensitive silverhalide emulsion layers.(21) The silver halide color photographic light-sensitive materialaccording to the item (20) above, wherein the yellow color-forminglight-sensitive silver halide emulsion layer is provided on a sideclosest to the support.(22) The silver halide color photographic light-sensitive materialaccording to any one of the items (19) to (21) above, wherein the totalcoating amount of silver is 0.25 g/m² or more and 0.50 g/m² or less.(23) The silver halide color photographic light-sensitive materialaccording to any one of the items (19) to (22) above, wherein the silverhalide emulsion in each of the silver halide emulsion layers containscubic grains with an average side length of 0.10 μm or more and 0.50 μmor less.(24) The silver halide color photographic light-sensitive materialaccording to any one of the items (19) to (23) above, wherein ahydrophilic binder in photographic constituent layers is in a totalcoating amount of 4.0 g/m² or more and 5.7 g/m² or less.(25) The silver halide color photographic light-sensitive materialaccording to any one of the items (19) to (24) above, which has awater-swelling rate of 200% or more and 300% or less.(26) The silver halide color photographic light-sensitive materialaccording to any one of the items (19) to (25) above, whereinphotographic constituent layers have a film thickness of 5.0 μm or moreand 7.7 μm or less.(27) A method of forming an image, comprising, subjecting the silverhalide color photographic light-sensitive material according to any oneof the items (19) to (26) above, to development processing with a colordeveloper containingN-ethyl-N-(β-methanesulfonamidoethyl)-3-methyl-4-aminoaniline.(28) A method of forming an image, comprising, subjecting the silverhalide color photographic light-sensitive material according to any oneof the items (19) to (27) above, to scanning exposure for an exposuretime of 1×10⁻³ second or less per pixel, and to color-developmentprocessing.

(Hereinafter, a fourth embodiment of the present invention means toinclude the silver halide color photographic light-sensitive materialsor the methods of forming an image, as described in the items (19) to(28) above.)

Herein, the present invention means to include all of the above first,second, third and fourth embodiments, unless otherwise specified.

In the present invention, preferably in the first embodiment,Dmax(UV)/Dmin(UV), which is defined as described above, is measured asfollows.

A sample subjected to exposure to white light of a color temperature of4,800° K. through a sharp cut filter SC-39 (trade name, which can cutlight having a wavelength shorter than 390 nm) manufactured by FujiPhoto Film Co., Ltd., for an exposure time of 1 second at an exposureamount of 2,000 CMS, and an unexposed sample were each subjected tocolor development processing as described below. These two samples,exposed and unexposed, are measured for color density by the methoddescribed below. Of the values obtained, one measured for the samplehaving a higher color density is defined as Dmax, and the other measuredfor the sample having a lower color density is defined as Dmin.

The above color-development processing utilizes a color developer ifnecessary, and the followings can be mentioned as the processing: in thecase where a transmission (transmitting) negative-type colorphotographic light-sensitive material is used, the developmentprocessing described in Example 1-1 hereinbelow; in the case where atransmitting positive-type color photographic light-sensitive materialis used, the development processing-CR described in Example 1-4hereinbelow; in the case where a reflective support color photographiclight-sensitive material is used, the development processing A describedin Example 1-5 hereinbelow.

(Measuring Method for Dmax and Dmin)

By using 10 cm² of each sample after the processing, the gelatin in thephotographic constituent layer is enzymatically decomposed with 20 ml ofwater containing 5 mg of actinase at 40° C., for 60 minutes, to elutethe photographic constituent layer. After cooling the eluate at 25° C.,it is treated with 20 ml of ethyl acetate, to extract oil-solublecomponents. The extract is once dried up by use of a rotary evaporatorunder the conditions of 40° C. under reduced pressure, and the finalamount of the extract is made to be 10 ml with ethyl acetate containing0.3 mass % of acetic acid in a volumetric flask. The operations ofpreparing a solution from the enzymatic decomposition with actinase tothis step are performed under light-shielded conditions. This solutionwas measured for absorption spectra at 340 nm to 450 nm in a 1-cm thicksilica cell, and Dmax(UV)/Dmin(UV) defined below is determined bycalculation. Herein, the term “a portion having the yellow maximum colordensity” means a portion of a sample, which is one of the two samples,exposed or unexposed, and which has a higher color density attained byusing a color forming yellow coupler. Herein, the term “a portion havingthe yellow minimum color density” means a portion of a sample, which isanother of the two samples, exposed or unexposed, and which has a lowercolor density obtained by not allowing or by allowing a color-formingyellow coupler to form color. Definition of Dmax(UV)/Dmin(UV): “thesmallest value in a range of wavelength UV, in which UV is a wavelengthwithin the range of 340 nm or more and 450 nm or less, among valuesrepresented by (an absorbance at a wavelength UV, for a portion havingthe yellow maximum color density)/(an absorbance at the wavelength UV,for a portion having the yellow minimum color density).” For example,when the value Dmax(UV)/Dmin(UV) has the smallest value 0.5 at 400 nm,Dmax(UV)/Dmin(UV) is represented by Dmax(400 nm/Dmin(400 nm)=0.5.

In the present invention, preferably in the first embodiment, the rangeof Dmax(UV)/Dmin(UV) is preferably 0.50 or more and 1.10 or less, morepreferably 0.5 or more and 0.9 or less, still more preferably 0.6 ormore and 1.0 or less, most preferably 0.7 or more and 0.9 or less.

The greater the value of Dmin(UV) (on this occasion, the value ofDmax(UV)/Dmin(UV) becomes smaller) is, the less the static-induced fogtends to be, which is preferable. However, in the case whereDmax(UV)/Dmin(UV) is smaller than 0.5, there arises an undesirably largeharmful influence that a molar extinction coefficient of the dye formedby coupling with an oxidized developing agent is small or thatabsorption of the coupler gives yellow tint to the photographiclight-sensitive material after processing.

In the present invention, preferably in the first embodiment, it ispreferred that the value defined by (B−C)/A be within theabove-mentioned specific range. Hereinafter, the measuring methodthereof is described. An unexposed sample and a sample subjected toexposure to white light of a color temperature 4,800° K in a yellowcoupler containing silver halide emulsion layer through a sharp cutfilter SC-39 (trade name) manufactured by Fuji Photo Film Co., Ltd., foran exposure time of 1 second at an exposure amount of 2,000 CMS (1× sec)were each subjected to color-development processing as described above.By using the yellow density B at the portion showing the maximum colordensity and the minimum yellow color density C and by using the amountto be used (coating amount) of the compound represented by formula (I),A mol/m², (B−C)/A is determined by calculation. The densitometer usedis, for example, HPD Densitometer (trade name, manufactured by FijiPhoto Film Co., Ltd., 436 nm, a reflection light measuring densitometer)in the case of a reflective support photosensitive material, and SCDDensitometer (trade name, manufactured by Fuji Photo Film Co., Ltd., atransmission light measuring densitometer) in the case of a transmittingsupport photosensitive material.

In the present invention, preferably in the first embodiment, when atransmitting support is used, (B−C)/A is preferably 1,300 or more and10,000 or less, more preferably 1,700 or more and 10,000 or less, stillmore preferably 1,800 or more and 8,000 or less, and most preferably1,900 or more and 4,000 or less.

In the present invention, preferably in the first embodiment, when areflective support photosensitive material is used, (B−C)/A ispreferably 4,200 or more and 20,000 or less, more preferably 4,500 ormore and 10,000 or less, and most preferably 4,600 or more and 6,500 orless.

In the present invention, preferably in the first embodiment, the yellowcoupler represented by formula (I) may be used as a mixture with anotheryellow coupler in an arbitrary ratio. The ratio of the yellow couplerfor use in the present invention in terms of mol ratio is preferably 10%or more, more preferably 25% or more, still more preferably 50% or more,and most preferably 75% or more and 100% or less.

The present invention is explained below in detail.

(Dye-Forming Coupler)

The compounds (referred to also as a dye-forming coupler or a yellowdye-forming coupler in the present specification) represented by formula(I) for use in the present invention is explained in detail.

In formula (I), R1 represents a substituent other than a hydrogen atom.Examples of the substituent include a halogen atom, an alkyl group(including a cycloalkyl group and a bicycloalkyl group), an alkenylgroup (including a cycloalkenyl group and a bicycloalkenyl group), analkynyl group, an aryl group, a heterocyclic group, a cyano group, ahydroxyl group, a nitro group, a carboxyl group, an alkoxy group, anaryloxy group, a silyloxy group, a heterocyclic oxy group, an acyloxygroup, a carbamoyloxy group, an alkoxycarbonyloxy group, anaryloxycarbonyloxy group, an amino group (including an alkylamino groupand an anilino group), an acylamino group, an aminocarbonylamino group,an alkoxycarbonylamino group, an aryloxycarbonylamino group, asulfamoylamino group, an sulfonamido group (including an alkyl- oraryl-sulfonylamino group), a mercapto group, an alkylthio group, anarylthio group, a heterocyclic thio group, a sulfamoyl group, a sulfogroup, an alkyl- or aryl-sulfinyl group, an alkyl- or aryl-sulfonylgroup, an acyl group, an aryloxycarbonyl group, an alkoxycarbonyl group,a carbamoyl group, an aryl- or heterocyclic-azo group, an imido group, aphosphino group, a phosphinyl group, a phosphinyloxy group, aphosphinylamino group, and a silyl group.

The above-mentioned substituent may be further substituted with anothersubstituent, and examples of this another substituent are the same tothe above-mentioned examples of the substituent.

R1 is preferably a substituted or unsubstituted alkyl group. The totalnumber of carbon atoms of R1 is preferably in the range of 1 to 60, morepreferably in the range of 6 to 50, still more preferably in the rangeof 11 to 40, and most preferably in the range of 16 to 30. In the casewhere R1 is a substituted alkyl group, examples of the substituent onthe alkyl group include those atoms and groups exemplified as thesubstituent of the above-mentioned R1.

The number of carbon atoms in the alkyl group itself represented by R1is preferably in the range of 1 to 40, more preferably in the range of 3to 36 and still more preferably in the range of 8 to 30-. Thispreferable order does not particularly depend on Q, but this order ispreferably applied in the case where Q described below is a grouprepresented by —C(—R11)=C(—R12)—CO—.

R1 is preferably an unsubstituted alkyl group having 11 or more carbonatoms, or an alkyl group substituted with an alkoxy group or aryloxygroup at the 2-, 3- or 4-position, more preferably an unsubstitutedalkyl group having 16 or more carbon atoms, or an alkyl groupsubstituted with an alkoxy group or aryloxy group at the 3-position, andmost preferably a C₁₆H₃₃ group, a C₁₈H₃₇ group, 3-lauryloxypropyl groupor 3-(2,4-di-t-amylphenoxy)propyl group.

In formula (I), Q represents a group of non-metal atoms necessary toform a 5- to 7-membered ring in combination with the —N═C—N(R1)—. The 5-to 7-membered ring thus formed is preferably a substituted orunsubstituted, and monocyclic or condensed heterocycle. More preferably,the ring-forming atoms are selected from carbon, nitrogen and sulfuratoms. Still more preferably, Q represents a group represented by—C(—R11)=C(—R12)—SO₂— or —C(—R11)=C(—R12)—CO— (in the present invention,these expressions of the foregoing groups do not limit the bondingorientation of the groups in formula (I), to the ones shown by theseexpressions). Q is preferably a group represented by—C(—R11)=C(—R12)—SO₂—. R11 and R12 represent groups that bond each otherto form a 5- to 7-membered ring together with the —C═C— moiety, or R11and R12 each independently represent a hydrogen atom or a substituent.The 5- to 7-membered ring thus formed may be saturated or unsaturated,and the ring may be an alicyclic, aromatic or heterocyclic ring.Examples of the ring include benzene, furan, thiophene, cyclopentane andcyclohexane rings. Further, examples of the substituent represented byR11 or R12 are those enumerated as the substituent of theabove-described R1.

These substituents and the ring formed through bonding of multiplesubstituents may be further substituted with another substituent(examples of this another substituent are the same as described as theexamples of the above-mentioned groups represented by R1).

In formula (I), R2 represents a substituent other than a hydrogen atom.Examples of the substituent are the same as those exemplified as thesubstituent represented by R1. R2 is preferably a halogen atom (e.g.,fluorine, chlorine, bromine), an alkyl group (e.g., methyl, isopropyl),an aryl group (e.g., phenyl, naphthyl), an alkoxy group (e.g., methoxy,isopropyloxy), an aryloxy group (e.g., phenoxy), an acyloxy group (e.g.,acetyloxy), an amino group (e.g., dimethylamino, morpholino), anacylamino group (e.g., acetoamido), a sulfonamido group (e.g.,methanesulfonamido, benzenesulfonamido), an alkoxycarbonyl group (e.g.,methoxycarbonyl), an aryloxycarbonyl group (e.g., phenoxycarbonyl), acarbamoyl group (e.g., N-methylcarbamoyl, N,N-diethylcarbamoyl), asulfamoyl group (e.g., N-methylsulfamoyl, N,N-diethylsulfamoyl), analkylsulfonyl group (e.g., methanesulfonyl), an arylsulfonyl group(e.g., benzenesulfonyl), an alkylthio group (e.g., methylthio,dodecylthio), an arylthio group (e.g., phenylthio, naphthylthio), acyano group, a carboxyl group, or a sulfo group. When R2 is at the orthoposition to the —CONH— group, R2 is preferably a halogen atom, an alkoxygroup, an aryloxy group, an alkyl group, an alkylthio group, or anarylthio group.

In the present invention, it is preferable that at least one R2 is atthe ortho position to the —CONH— group.

In formula (I), m represents an integer of 0 to 5. When m is 2 or more,R_(2s) may be the same or different, or R2s may bond with each other toform a ring.

m is preferably an integer of 0 to 3, more preferably 0 to 2, still morepreferably 1 to 2, and most preferably 2.

In formula (I), X represents a hydrogen atom, or a group that is capableof being split-off upon a coupling reaction with an oxidized product ofa developing agent. Examples of the group, represented by X, capable ofbeing split-off upon a coupling reaction with an oxidized product of adeveloping agent, include a group capable of being split-off with anitrogen, oxygen, or sulfur atom (a splitting-off atom), and a halogenatom (e.g., chlorine, bromine).

Examples of the group that splits off with a nitrogen atom include aheterocyclic group (preferably a 5- to 7-membered substituted orunsubstituted, saturated or unsaturated, aromatic (herein the term“aromatic” is used to embrace a substance that has (4n+2) cyclicconjugated electrons) or non-aromatic, monocyclic or condensedheterocyclic groups, more preferably a 5- to 6-membered heterocyclicgroup, in which the ring-forming atoms are selected from carbon,nitrogen and sulfur atoms and in addition at least one of hetero atomsselected from nitrogen, oxygen and sulfur atoms is incorporated, withspecific examples of the heterocyclic group including succinimide,maleinimide, phthalimide, diglycolimide, pyrrole, pyrazole, imidazole,1,2,4-triazole, tetrazole, indole, benzopyrazole, benzimidazole,benzotriazole, imidazoline-2,4-dione, oxazolidine-2,4-dione,thiazolidine-2-one, benzimidazoline-2-one, benzoxazoline-2-one,benzothiazoline-2-one, 2-pyrroline-5-one, 2-imidazoline-5-one,indoline-2,3-dione, 2,6-dioxypurine parabanic acid,1,2,4-triazolidine-3,5-dione, 2-pyridone, 4-pyridone, 2-pyrimidone,6-pyridazone, 2-pyrazone, 2-amino-1,3,4-thiazolidine-4-one), acarbonamido group (e.g., acetamido, trifluoroacetamido), a sulfonamidogroup (e.g., methanesulfonamido, benzenesulfornamido), an arylazo group(e.g., phenylazo, naphthylazo), and a carbamoylamino group (e.g.,N-methyl carbamoylamino).

Preferred of the group that splits off with a nitrogen atom areheterocyclic groups, more preferably aromatic heterocyclic groups having1, 2, 3, or 4 nitrogen atom(s) as ring-forming atoms, or heterocyclicgroups represented by the following formula (L).

In formula (L), L represents a moiety that forms, together with the—NC(═O)—, a 5- to 6-membered nitrogen-containing heterocycle.

Examples of the moieties are enumerated in the explanation of theabove-mentioned heterocyclic group, and such moieties as enumeratedabove are more preferred.

Particularly preferably L is a moiety that forms a 5-memberednitrogen-containing heterocycle.

Examples of the group that splits off with an oxygen atom include anaryloxy group (e.g., phenoxy, 1-naphthoxy), a heterocyclic oxy group(e.g., pyridyloxy, pyrazolyloxy), an acyloxy group (e.g., acetoxy,benzoyloxy), an alkoxy group (e.g., methoxy, dodecyloxy), a carbamoyloxygroup (e.g., N,N-diethylcarbamoyloxy, morpholinocarbamoyloxy), anaryloxycarbonyloxy group (e.g., phenoxycarbonyloxy), analkoxycarbonyloxy group (e.g., methoxycarbonyloxy, ethoxycarbonyloxy),an alkylsulfonyloxy group (e.g., methanesulfonyloxy), and anarylsulfonyloxy group (e.g., benzenesulfonyloxy, toluenesulfonyloxy).

Preferred of the group that splits off with an oxygen atom are anaryloxy group, an acyloxy group, and a heterocyclic oxy group.

Examples of the group that splits off with a sulfur atom include anarylthio group (e.g., phenylthio, naphthylthio), a heterocyclic thiogroup (e.g., tetrazolylthio, 1,3,4-thiadiazolylthio, 1,3,4-oxazolylthio,benzimidazolylthio), an alkylthio group (e.g., methylthio, octylthio,hexadecylthio), an alkylsulfinyl group (e.g., methanesulfinyl), anarylsulfinyl group (e.g., benzenesulfinyl), an arylsulfonyl group (e.g.,benzenesulfonyl), and an alkylsulfonyl group (e.g., methanesulfonyl).

Preferred of the group that splits off with a sulfur atom are anarylthio group and a heterocyclic thio group. A heterocyclic thio groupis more preferred.

X may be substituted with a substituent. Examples of the substituentsubstituting on X include those enumerated as the substituentrepresented by R1.

X is preferably a group capable of being split-off upon a couplingreaction with an oxidized product of a developing agent, more preferablya group that can split off with a nitrogen atom, a group that can splitoff with an oxygen atom or a group that can split off with a sulfuratom, still more preferably a group that can split off with a nitrogenatom. Further preferably, the split-off group is the above-mentionedpreferable examples for the group that splits off with a nitrogen atom,and they are preferable in the described order.

Preferable examples of X are explained in more detail below. The groupthat can split off with a nitrogen is preferable; and an aromaticheterocyclic group having at least two nitrogen atoms (preferably 2)(preferably a 5-membered aromatic heterocyclic group, such as a pyrazolegroup, optionally having a substituent) and a group represented by theabove-mentioned formula (L) are particularly preferable.

X may be a group to give a photographically useful substance. Examplesof the photographically useful substance include a developmentinhibitor, a desilvering accelerator, a redox compound, a dye, a couplerand the like, as well as their precursors.

In the present invention, it is preferable that X is not theabove-described group to give a photographically useful substance.

In order to render the coupler immobile in the light-sensitive material,at least one of Q, R1, X and R2 has preferably 8 to 50 carbon atoms,more preferably 10 to 40 carbon atoms in total respectively, includingcarbon atoms of a substituent(s) that they may have.

Among the compounds represented by the formula (I) for use in thepresent invention, preferable compounds can be represented by formula(II).

The compounds (referred to also as a dye-forming coupler in the presentspecification) represented by formula (II) for use in the presentinvention is explained in detail.

In formula (II), R1, R2, m and X each have the same meanings as thosedescribed in formula (I). Preferable ranges thereof are also the same.

In formula (II), R3 represents a substituent. Examples of thesubstituent are the same as those exemplified above as the substituentrepresented by R1. R3 is preferably a halogen atom (e.g., fluorine,chlorine, bromine), an alkyl group (e.g., methyl, isopropyl), an arylgroup (e.g., phenyl, naphthyl), an alkoxy group (e.g., methoxy,isopropyloxy), an aryloxy group (e.g., phenoxy), an acyloxy group (e.g.,acetyloxy), an amino group (e.g., dimethylamino, morpholino), anacylamino group (e.g., acetoamide), an sulfonamido group (e.g.,methanesulfonamido, benzenesulfonamido), an alkoxycarbonyl group (e.g.,methoxycarbonyl), an aryloxycarbonyl group (e.g., phenoxycarbonyl), acarbamoyl group (e.g., N-methylcarbamoyl, N,N-diethylcarbamoyl), asulfamoyl group (e.g., N-methylsulfamoyl, N,N-diethylsulfamoyl), analkylsulfonyl group (e.g., methanesulfonyl), an arylsulfonyl group(e.g., benzenesulfonyl), a cyano group, a carboxyl group, or a sulfogroup.

n represents an integer of 0 to 4. When n is 2 or more, the plurality ofR3s may be the same or different, and the R3s may bond with each otherto form a ring.

In the present invention, preferably in the first embodiment, as thecoupler represented by formula (I), a coupler, whose ultravioletabsorption density is high before color-forming (around the wavelengthrange of 340 nm to 400 nm), in which a molar extinction coefficient of adye formed after color-forming is high, and in which ultravioletabsorption mentioned in the above is lower than coupler absorptionbefore color-forming, is particularly preferably used.

Preferred specific examples of the couplers represented by formula (I)or (II) according to the present invention are shown below, but thepresent invention is not limited to these examples. Herein, the presentinvention also includes tautomers, in which the hydrogen atom at thecoupling site (the hydrogen atom on the carbon atom to which X issubstituting) is transferred on the nitrogen atom in the C═N portionbonding to the coupling site (the ring-constituting nitrogen atom thatis not bonded with R1).

In the present specification, Me means a methyl group, Et means an ethylgroup, and Ph means a phenyl group, respectively.

When any one of the exemplified compounds (which may also be referred toas a dye-forming coupler) shown above is referred to in the followingdescription, a number X put in parentheses, that is, (X) attached to theexemplified compound is used to express the compound as “coupler (X)”.

Specific synthetic examples of the compounds represented by theforegoing formula (I) and (II) are described below.

Synthetic Example 1 Synthesis of Coupler (1)

Coupler (1) was synthesized according to the following synthesis route:

44.3 g of o-nitrobenzenesulfonyl chloride was gradually added, withstirring, to a mixture solution of 38.8 g of an aqueous 40% methylaminesolution and 200 ml of acetonitrile, on an ice bath. The resultingreaction mixture was heated up to room temperature and stirred foranother 1 hour. Thereafter, ethyl acetate and water were added, and theorganic layer was separated from the aqueous layer. The organic layerwas washed with dilute hydrochloric acid and then a saturated brine.After the organic layer was dried with magnesium sulfate anhydride, thesolvent was removed by vacuum distillation. Crystallization from a mixedsolvent of ethyl acetate and hexane gave 28.6 g of Compound (A-1).

44.8 g of reduced iron and 4.5 g of ammonium chloride were dispersed ina mixture of 270 ml of isopropanol and 45 ml of water, and heated for 1hour under refluxing. To the resulting mixture, 25.9 g of Compound (A-1)was gradually added with stirring. After heating in refluxing foranother 1 hour, insoluble matters were removed by a suction filtrationthrough Celite. Ethyl acetate and water were added to the filtrate, andthe organic layer was separated from the aqueous layer. The organiclayer was washed with a saturated brine, and then dried with magnesiumsulfate anhydride. The solvent was removed by vacuum distillation, toyield 21.5 g of Compound (A-2) as an oily product.

A solution of 18.9 g of Compound (A-2), 39.1 g of hydrochloride ofiminoether (A-0) and 200 ml of ethyl alcohol was stirred with heating inrefluxing for 1 day. Further, 19.2 g of hydrochloride of iminoether wasadded and stirred with heating in refluxing for another 1 day. Ethylacetate and water were added, and the organic layer was separated fromthe aqueous layer. The organic layer was washed with dilute hydrochloricacid and a saturated brine, and then dried with magnesium sulfateanhydride. The solvent was removed by vacuum distillation.Crystallization from a mixed solvent of ethyl acetate and hexane gave21.0 g of Compound (A-3).

A solution of 5.6 g of Compound (A-3), 7.2 g of2-methoxy-5-tetradecyloxycarbonylaniline and 20 ml of m-dichlorobenzenewas stirred with heating in refluxing for 6 hours. After cooling,crystallization by adding hexane gave 8.8 g of Compound (A-4).

To 110 ml of methylene chloride solution containing 5.4 g of Compound(A-4), 10 ml of methylene chloride solution containing 0.45 ml ofbromine was added drop-wise on an ice bath. After the resultant mixturewas stirred for 30 minutes at room temperature, methylene chloride andwater were added, and the organic layer was separated from the aqueouslayer. The organic layer was washed with a saturated brine, and thendried with magnesium sulfate anhydride. The solvent was removed byvacuum distillation, to obtain a crude product of Compound (A-5).

To a solution which was prepared by dissolving 3.5 g of5,5-dimethyloxazolidine-2,4-dione and 3.8 ml of triethylamine in 110 mlof N,N-dimethyl acetoamide, a solution containing all the previouslysynthesized crude product of Compound (A-5) dissolved in 25 ml ofacetonitrile was added drop-wise over 10 minutes at room temperature,and then stirred for 2 hours at room temperature. Ethyl acetate andwater were added, and the organic layer was separated from the aqueouslayer. The organic layer was washed with 0.1 normal aqueous potassiumhydroxide solution, dilute hydrochloric acid and a saturated brine, andthen dried with magnesium sulfate anhydride. The solvent was removed byvacuum distillation. The residue was purified on silica gel columnchromatography using a mixed solvent of acetone and hexane as an eluate,and then recrystallized from a mixed solvent of ethyl acetate andhexane, to give 4.7 g of Coupler (1).

Synthetic Example 2 Synthesis of Coupler (3)

Coupler (3) was synthesized according to the following synthesis route:

To a solution containing 438 g of 3-(2,4-di-t-amylphenoxy) propylamine,210 ml of triethylamine and 1 liter of acetonitrile, 333 g ofo-nitrobenzenesulfonyl chloride was gradually added with stirring on anice bath. The resulting reaction mixture was heated up to roomtemperature and further stirred for 1 hour. Thereafter, ethyl acetateand water were added, and the organic layer was separated from theaqueous layer. The organic layer was washed with dilute hydrochloricacid and a saturated brine. After the organic layer was dried withmagnesium sulfate anhydride, the solvent was removed by vacuumdistillation. Crystallization from a mixed solvent of ethyl acetate andhexane gave 588 g of Compound (B-1).

84.0 g of reduced iron and 8.4 g of ammonium chloride were dispersed ina mixture of 540 ml of isopropanol and 90 ml of water, and heated inrefluxing for 1 hour. To the resulting dispersion, 119 g of Compound(B-1) was gradually added with stirring. After heating in refluxing foranother 2 hours, the reaction mixture was filtrated by a suctionfiltration through Celite. Ethyl acetate and water were added to thefiltrate, and the organic layer was separated from the aqueous layer.The organic layer was washed with a saturated brine, and then dried withmagnesium sulfate anhydride. The solvent was removed by vacuumdistillation, to yield 111 g of Compound (B-2) as an oily product.

A solution of 111 g of Compound (B-2), 68.4 g of hydrochloride ofiminoether (A-0) and 150 ml of ethyl alcohol was stirred with heating inrefluxing for 1 hour. Additionally 4.9 g of hydrochloride of iminoetherwas added and stirred with heating in refluxing for 30 minutes. Aftercooling the reaction mixture, it was filtered under suction, 100 ml ofp-xylene was added to the filtrate and then heated in refluxing for 4hours while removing ethyl alcohol by distillation. The reactionsolution was purified by a silica gel column chromatography using amixed solvent of ethyl acetate and hexane as the eluate. Crystallizationfrom methanol gave 93.1 g of Compound (B-3).

A solution of 40.7 g of Compound (B-3), 18.5 g of 2-methoxyaniline and10 ml of p-xylene was stirred with heating in refluxing for 6 hours.Ethyl acetate and water were added, and the organic layer was separatedfrom the aqueous layer. The organic layer was washed with dilutehydrochloric acid and a saturated brine, and then dried with magnesiumsulfate anhydride. The solvent was removed by vacuum distillation.Purification of the residue by a silica gel column chromatography usinga mixed solvent of ethyl acetate and hexane as the eluate gave 37.7 g ofCompound (B-4) as an oily product.

To a solution of 24.8 g of Compound (B-4) in 400 ml of methylenechloride, 35 ml of methylene chloride solution containing 2.1 ml ofbromine was added drop-wise on an ice bath. After the mixture wasstirred for 30 minutes on an ice bath, methylene chloride and water wereadded, and the organic layer was separated from the aqueous layer. Theorganic layer was washed with a saturated brine, and then dried withmagnesium sulfate anhydride. The solvent was removed by vacuumdistillation, to obtain Compound (B-5) as a crude product.

To a solution of 15.5 g of 5,5-dimethyl oxazolidine-2,4-dione and 16.8ml of triethylamine in 200 ml of N,N-dimethyl acetoamide, a solutioncontaining all the previously synthesized crude product of Compound(B-5) dissolved in 40 ml of acetonitrile was added drop-wise over 10minutes at room temperature. The resultant mixture was heated up to 40°C. and then stirred for 30 minutes. Ethyl acetate and water were added,and the organic layer was separated from the aqueous layer. The organiclayer was washed with 0.1 normal aqueous potassium hydroxide solution,dilute hydrochloric acid and a saturated brine, and then dried withmagnesium sulfate anhydride. The solvent was removed by vacuumdistillation. The residue was purified by a silica gel columnchromatography using a mixed solvent of acetone and hexane as theeluate. Crystallization from a mixed solvent of ethyl acetate and hexanegave 23.4 g of Coupler (3).

Synthetic Example 3 Synthesis of Coupler (6)

Coupler (6) was synthesized according to the following synthesis route:

To a solution of 21.4 g of benzylamine in 200 ml of acetonitrile, 39.9 gof o-nitrobenzenesulfonyl chloride was gradually added with stirring onan ice bath. The resulting reaction mixture was heated up to roomtemperature. Further, 30 ml of triethylamine was added drop-wise andstirred for 1 hour. Thereafter, ethyl acetate and water were added, andthe organic layer was separated from the aqueous layer. The organiclayer was washed with dilute hydrochloric acid and then a saturatedbrine. After the organic layer was dried with magnesium sulfateanhydride, the solvent was removed by vacuum distillation.Crystallization from a mixed solvent of ethyl acetate and hexane gave31.2 g of Compound (C-1).

44.8 g of reduced iron and 4.5 g of ammonium chloride were dispersed ina mixture of 270 ml of isopropanol and 45 ml of water, and heated for 1hour in refluxing. To the resulting mixture, 29.2 g of Compound (C-1)was gradually added with stirring. After heating in refluxing foranother 1 hour, the reaction mixture was filtrated by a suctionfiltration through Celite. Ethyl acetate and water were added to thefiltrate, and the organic layer was separated from the aqueous layer.The organic layer was washed with a saturated brine, and then dried withmagnesium sulfate anhydride. The solvent was removed by vacuumdistillation, to yield 25.5 g of Compound (C-2) as an oily product.

A solution of 19.7 g of Compound (C-2) and 22.0 g of hydrochloride ofiminoether (A-0) in 200 ml of ethyl alcohol was stirred with heating inrefluxing for 4 hours. Further, 19.7 g of hydrochloride of theiminoether was added and stirred with heating under reflux for 4 hours.Additionally 13 g of p-toluene sulfonic acid monohydrate was added andstirred with heating in refluxing for 1 hour. Ethyl acetate and waterwere added, and the organic layer was separated from the aqueous layer.The organic layer was washed with dilute hydrochloric acid and asaturated brine, and then dried with magnesium sulfate anhydride. Thesolvent was removed by vacuum distillation. Crystallization from a mixedsolvent of ethyl acetate and hexane gave 3.2 g of Compound (C-3).

A solution of 2.9 g of Compound (C-3), 2.9 g of2-methoxy-5-tetradecyloxycarbonylaniline in 20 ml of o-dichlorobenzenewas stirred for 6 hours with heating in refluxing. Ethyl acetate andwater were added, and the organic layer was separated from the aqueouslayer. The organic layer was washed with dilute hydrochloric acid and asaturated brine, and then dried with magnesium sulfate anhydride. Thesolvent was removed by vacuum distillation. The residue was purified bya silica gel column chromatography using a mixed solvent of ethylacetate and hexane as the eluate. Crystallization from a mixed solventof ethyl acetate and hexane gave 3.8 g of Compound (C-4).

To a solution containing 3.4 g of Compound (C-4) in 100 ml of methylenechloride, 10 ml of methylene chloride solution containing 0.26 ml ofbromine was added drop-wise on an ice bath. After the mixture wasstirred for 30 minutes at room temperature, methylene chloride and waterwere added, and the organic layer was separated from the aqueous layer.The organic layer was washed with a saturated brine, and then dried withmagnesium sulfate anhydride. The solvent was removed by vacuumdistillation, to obtain a crude product of Compound (C-5).

To a solution of 3.5 g of 1-benzyl-5-ethoxyhydantoin and 2.1 ml oftriethylamine in 100 ml of N,N-dimethyl acetoamide, a solutioncontaining all the previously synthesized crude product of Compound(C-5) dissolved in 20 ml of acetonitrile was added drop-wise over 30minutes at room temperature, and then stirred at 40° C. for 2 hours.Ethyl acetate and water were added, and the organic layer was separatedfrom the aqueous layer. The organic layer was washed with 0.1 normalaqueous potassium hydroxide solution, dilute hydrochloric acid and asaturated brine, and then dried with magnesium sulfate anhydride. Thesolvent was removed by vacuum distillation. The residue was purified bya silica gel column chromatography using a mixed solvent of ethylacetate and hexane as the eluate. Crystallization from a mixed solventof ethyl acetate and hexane gave 3.0 g of Coupler (6).

Synthetic Example 4 Synthesis of Coupler (11)

Coupler (11) was synthesized according to the following synthesis route:

To a solution of 26.8 g of Compound (D-0) (Coupler-I described in U.S.Pat. No. 3,841,880) and 16.6 g of potassium carbonate in 300 ml ofacetone, 13.9 g of dimethyl sulfate was added drop-wise and stirred for2 hours with heating in refluxing. Ethyl acetate and water were added,and the organic layer was separated from the aqueous layer. The organiclayer was washed with dilute hydrochloric acid and a saturated brine,and then dried with magnesium sulfate anhydride. The solvent was removedby vacuum distillation. The residue was purified by a silica gel columnchromatography using a mixed solvent of acetone and hexane as theeluate. Crystallization from a mixed solvent of ethyl acetate and hexanegave 5.6 g of Compound (D-1). At the same time, 10.9 g of Compound (A-3)was obtained as a by-product. Coupler (1) may be synthesized usingCompound (A-3) thus prepared.

A solution of 5.4 g of Compound (D-1) and 7.3 g of2-methoxy-5-tetradecyloxycarbonylaniline in 50 ml of o-dichlorobenzenewas stirred for 6 hours with heating in refluxing. Ethyl acetate andwater were added, and the organic layer was separated from the aqueouslayer. The organic layer was washed with dilute hydrochloric acid and asaturated brine, and then dried with magnesium sulfate anhydride. Thesolvent was removed by vacuum distillation. Crystallization from a mixedsolvent of ethyl acetate and methanol gave 9.1 g of Compound (D-2).

To a solution of 4.8 g of Compound (D-2) in 100 ml of methylenechloride, 10 ml of a methylene chloride solution containing 0.4 ml ofbromine was added drop-wise on an ice bath. The reaction mixture wasstirred for 30 minutes on an ice bath. Thereafter, methylene chlorideand water were added, and the organic layer was separated from theaqueous layer. The organic layer was washed with a saturated brine, andthen dried with magnesium sulfate anhydride. The solvent was removed byvacuum distillation, to obtain a crude product of Compound (D-3).

To a solution of 3.8 g of 5-butyloxazolidine-2,4-dione and 3.4 ml oftriethylamine dissolved in 100 ml of N,N-dimethyl acetamide, a solutioncontaining all the previously synthesized crude product of Compound(D-3) dissolved in 50 ml of N,N-dimethylacetamide was added drop-wise atroom temperature over 30 minutes, and the resultant mixture was stirredfor 1 hour at room temperature. Ethyl acetate and water were added, andthe organic layer was separated from the aqueous layer. The organiclayer was washed with 0.1 normal aqueous potassium hydroxide solution,dilute hydrochloric acid and a saturated brine, and then dried withmagnesium sulfate anhydride. The solvent was removed by vacuumdistillation. The residue was purified by a silica gel columnchromatography using a mixed solvent of acetone, tetrahydrofuran, andhexane as the eluate. Crystallization from a mixed solvent of ethylacetate and hexane gave 2.1 g of Coupler (11).

Synthetic Example 5 Synthesis of Coupler (13)

Coupler (13) was synthesized in the synthesis route shown below.

32.2 g of benzylamine was added, drop-wise, to 200 ml of an acetonitrilesolution containing 48.9 g of isatoic acid anhydride, and the resultingmixture was stirred. The resulting mixture was heated up to 60° C. andfurther stirred for 10 minutes. Thereafter, ethyl acetate and water wereadded thereto, and the organic layer was separated from the aqueouslayer. The organic layer was dried with magnesium sulfate anhydride, andthen the solvent was removed by vacuum distillation. Crystallizationfrom a mixed solvent of ether and hexane gave 54.6 g of Compound (E-1).

200 ml of an ethyl alcohol solution containing 24.9 g of Compound (E-1),21.6 g of hydrochloride of iminoether (A-0) and 10.5 g ofp-toluenesulfonic acid monohydrate was stirred for 3 hours with heatingunder reflux. After cooling, 21.6 g of hydrochloride of iminoether wasadded and further stirred with heating under reflux for 1 hour. Ethylacetate and water were added, and the organic layer was separated fromthe aqueous layer. The organic layer was dried with magnesium sulfateanhydride. The solvent was removed by vacuum distillation.Crystallization from a mixed solvent of ether and hexane gave 33.6 g ofCompound (E-2).

50 ml of p-xylene solution containing 6.5 g of Compound (E-2) and 6.5 gof 2-chloro-5-dodecyloxycarbonylaniline was stirred for 2 hours withheating under reflux. Further, 0.2 g of p-toluenesulfonic acidmonohydrate was added and stirred for 4 hours with heating under reflux.Ethyl acetate and water were added, and the organic layer was separatedfrom the aqueous layer. The organic layer was washed with 1-normalaqueous solution of hydrochloric acid and a saturated brine, and thendried with magnesium sulfate anhydride. The solvent was removed byvacuum distillation. Crystallization from a mixed solvent of ethylacetate and hexane gave 6.7 g of Compound (E-3).

To 70 ml of a methylene chloride solution containing 5.5 g of Compound(E-3), 15 ml of a methylene chloride solution containing 0.48 ml ofbromine was added drop-wise under cooling with ice. After the mixturewas stirred at room temperature for 30 minutes, methylene chloride andwater were added, and the organic layer was separated from the aqueouslayer. The organic layer was washed with a saturated brine, and thendried with magnesium sulfate anhydride. The solvent was removed byvacuum distillation, to obtain a crude product of Compound (E-4).

To a solution which was prepared by dissolving 3.5 g of5,5-dimethyloxazolidine-2,4-dione and 3.8 ml of triethylamine in 50 mlof N,N-dimethyl acetoamide, a solution containing all the previouslysynthesized crude product of Compound (E-4) dissolved in 50 ml ofN,N-dimethyl acetoamide was added drop-wise over 10 minutes at roomtemperature, and then stirred for 1 hour at room temperature. Ethylacetate and water were added, and the organic layer was separated fromthe aqueous layer. The organic layer was washed with 1 normal aqueoussolution of potassium carbonate, 1 normal aqueous solution ofhydrochloric acid and a saturated brine, and then dried with magnesiumsulfate anhydride. The solvent was removed by vacuum distillation.Purification of the residue by silica gel column chromatography using amixed solvent of ethyl acetate and hexane as the eluate gave 4.0 g ofCoupler (13) as an amorphous product.

When the light-sensitive material of the present invention, preferablyof the first embodiment, is a transmission-type color photographiclight-sensitive material, it is enough for the light-sensitive materialto have at least one light-sensitive layer on a support. A typicalexample thereof is a silver halide photographic light-sensitive materialcomprising, on a support, at least one light-sensitive layer consistingof two or more silver halide emulsion layers whose color sensitivitiesare substantially the same, but whose light-sensitivities are differentfrom each other. Said light-sensitive layer is a unit light-sensitivelayer that has a color sensitivity to any of blue light, green light andred light. In a multi-layer silver halide color photographiclight-sensitive material, such unit light-sensitive layers are generallyarranged in the order of a red-sensitive layer, a green-sensitive layerand a blue-sensitive layer from the support side. However, according tothe intended use, this order of arrangement can be reversed.Alternatively, the layers may be arranged such that sensitive layerssensitive to the same color can sandwich another sensitive layersensitive to a different color. Non-sensitive layers can be provided asan interlayer between the silver halide light-sensitive layers, or asthe uppermost layer or the lowermost layer. These non-sensitive layerscan contain, for example, couplers, DIR compounds, and color-mixinginhibitors, which are described below. Each of the silver halideemulsion layers constituting unit photosensitive layers can preferablytake a two-layer constitution composed of a high-sensitive emulsionlayer and a low-sensitive emulsion layer, as described in DE 1 121 470or GB Patent No. 923 045. Generally, they are preferably arranged suchthat the sensitivities are decreased toward the support. As described,for example, in JP-A-57-112751, JP-A-62-200350, JP-A-62-206541, andJP-A-62-206543, a low-sensitive emulsion layer may be placed away fromthe support, and a high-sensitive emulsion layer may be placed nearer tothe support.

Specific examples of the order include an order of a low-sensitiveblue-sensitive layer (BL)/high-sensitive blue-sensitive layer(BH)/high-sensitive green-sensitive layer (GH)/low-sensitivegreen-sensitive layer (GL)/high-sensitive red-sensitive layer(RH)/low-sensitive red-sensitive layer (RL), or an order ofBH/BL/GL/GH/RH/RL, or an order of BH/BL/GH/GL/RL/RH, stated from theside most away from the support.

As described in JP-B-55-34932 (“JP-B” means examined Japanese patentpublication), an order of a blue-sensitive layer/GH/RH/GL/RL stated fromthe side most away from the support is also possible. Further asdescribed in JP-A-56-25738 and JP-A-62-63936, an order of ablue-sensitive layer/GL/RL/GH/RH stated from the side most away from thesupport is also possible.

Further as described in JP-B-49-15495, an arrangement is possiblewherein the upper layer is a silver halide emulsion layer highest insensitivity, the intermediate layer is a silver halide emulsion layerlower in sensitivity than that of the upper layer, the lower layer is asilver halide emulsion layer further lower in sensitivity than that ofthe intermediate layer, so that the three layers different insensitivity may be arranged with the sensitivities successively loweredtoward the support. Even in such a constitution comprising three layersdifferent in sensitivity, an order of a medium-sensitive emulsionlayer/high-sensitive emulsion layer/low-sensitive emulsion layer statedfrom the side away from the support may be taken in layers identical incolor sensitivity, as described in JP-A-59-202464.

Further, for example, an order of a high-sensitive emulsionlayer/low-sensitive emulsion layer/medium-sensitive emulsion layer, oran order of a low-sensitive emulsion layer/medium-sensitive emulsionlayer/high-sensitive emulsion layer stated from the side away fromsupport can be taken. In the case of four layers or more layers, thearrangement can be varied as above.

In order to improve color reproduction, as described in U.S. Pat. Nos.4,663,271, 4,705,744, and 4,707,436, and JP-A-62-160448 andJP-A-63-89850, it is preferable to form a donor layer (CL), which has aspectral sensitivity distribution different from those of a principal(main) light-sensitive layer, such as BL, GL and RL, and which has aninter-layer effect, in a position adjacent or in close proximity to theprincipal light-sensitive layer.

The silver halide that can be used in the present invention, preferablyin the first embodiment, is preferably silver iodobromide, silveriodochloride or silver iodochlorobromide, each containing about 30 mol %or less of silver iodide. The silver halide is particularly preferablysilver iodobromide or silver iodochlorobromide, each containing about 2mol % to about 10 mol % of silver iodide.

In the present invention, preferably in the first embodiment, silverhalide grains in the photographic emulsion may have any of variouscrystalline shapes. Examples of the crystalline shapes include regularcrystals, such as cubes, octahedrons, and tetradecahedrons; irregularcrystals, such as spherical crystals and tabular crystals; crystalshaving crystal defect such as twin plane; and a mixture of grains ofthese crystalline shapes.

The silver halide grains may be fine grains whose grain diameter isabout 0.2 μm or less, or large-size grains whose diameter of theprojected area is up to about 10 μm. The silver halide emulsion may be amonodispersed emulsion or a polydispersed emulsion.

The silver halide photographic emulsion that can be used in the presentinvention, preferably in the first embodiment, can be prepared, forexample, according to the methods described in Research Disclosure(hereinafter abbreviated to as RD) No. 17643 (December 1978), pp. 22-23,“I. Emulsion preparation and types”; RD No. 18716 (November 1979), p.648; RD No. 307105 (November 1989), pp. 863-865; by P. Glafkides in“Chemie et Phisique Photographique,” Paul Montel, 1967; by G. F. Duffinin “Photographic Emulsion Chemistry,” Focal Press, 1966; by V. L.Zelikman et al. in “Making and Coating of Photographic Emulsion,” FocalPress, 1964; and the like.

Monodispersed emulsions, described in U.S. Pat. Nos. 3,574,628 and3,655,349, and U.K. Patent No. 1,413,748, can also be preferably used.

Further, in the present invention, preferably in the first embodiment,use can be made of tabular grains whose aspect ratio is about 3 or more.In particular, for the purpose for improving preservability with thelapse of time, use can be preferably made of a silver halide emulsion,in which 50% or more of the projected area of all the silver halidegrains was occupied by tabular silver halide grains each having anaspect ratio of 8 or more.

There is no particular restriction on the upper limit of the aspectratio, but the aspect ratio is preferably 30 or less. The silver halideemulsion containing tabular grains may be easily prepared using each ofthe methods described, for example, by Gutoff, “Photographic Science andEngineering”, Vol. 14, pp. 248-257 (1970); in U.S. Pat. No. 4,434,226,No. 4,414,310, No. 4,433,048 and No. 4,439,520, and GB Patent No.2,112,157.

As to the crystal structure, a uniform structure, a structure in whichthe internal part and the external part have different halogencompositions, and a layered structure may be acceptable. Silver halidesdiffering in composition may be joined with each other by epitaxialjunction, and, for example, a silver halide may be joined with acompound other than silver halides, such as, silver rhodanate and leadoxide. Also, a mixture of grains having various crystalline shapes maybe used.

The silver halide emulsion may be any of a surface latent image-typeemulsion which predominantly forms a latent image on the surface of thesilver halide grain, an internal latent image-type emulsion whichpredominantly forms a latent image in the interior of the silver halidegrain, and another type of emulsion which forms a latent image both onthe surface and in the interior of the silver halide grain. However, theemulsion for use in the present invention, preferably in the firstembodiment, must be a negative type emulsion. The internal latent imagetype emulsion may be a core/shell internal latent image type emulsiondescribed in JP-A-63-264740. The method of preparing this core/shellinternal latent image type emulsion is described in JP-A-59-133542.Although the thickness of the shell of this emulsion depends on, forexample, development conditions, it is preferably 3 to 40 nm, andespecially preferably 5 to 20 nm.

The silver halide emulsion is generally subjected to physical ripening,chemical ripening, and spectral sensitization steps before it is used.Additives for use in these steps are described in R.D. Nos. 17643,18716, and 307105, and they are summarized in a table, which will beshown later. In the light-sensitive material of the present invention,preferably in the first embodiment, it is possible to mix, in a singlelayer, two or more types of emulsions different in at least one ofcharacteristics of a light-sensitive silver halide emulsion, i.e., agrain size, a grain size distribution, a halogen composition, a grainshape, and a sensitivity. It is preferable to apply surface-foggedsilver halide grains described in U.S. Pat. No. 4,082,553, internallyfogged silver halide grains described in U.S. Pat. No. 4,626,498 andJP-A-59-214852, or colloidal silver, in light-sensitive silver halideemulsion layers and/or substantially non-light-sensitive hydrophiliccolloid layers. The internally- or surface-fogged silver halide grainmeans a silver halide grain which can be developed uniformly (nonimage-wise) regardless of whether it exists at a non-exposed portion oran exposed portion of the light-sensitive material. A method ofpreparing the internally- or surface-fogged silver halide grain isdescribed in U.S. Pat. No. 4,626,498 and JP-A-59-214852. Silver halidesthat form the internal nuclei of an internally fogged core/shell typesilver halide grain may have different halogen compositions. As theinternally or surface-fogged silver halide, any of silver chloride,silver chlorobromide, silver iodobromide and silver chloroiodobromidecan be used. The average grain size of these fogged silver halide grainsis preferably 0.01 to 0.75 μm, and particularly preferably 0.05 to 0.6μm. The grain shape may be a regular grain shape. Although the emulsionmay be a polydisperse emulsion, it is preferably a monodisperse emulsion(in which at least 95% in mass or in the number of silver halide grainshave grain diameters falling within a range of ±40% of the average graindiameter).

In the present invention, preferably in the first embodiment, it ispreferable to use non-light-sensitive fine grain silver halide. Thenon-light-sensitive fine grain silver halide is a silver halide finegrain which is not sensitive to light during imagewise exposure forobtaining a dye image, and is not substantially developed duringprocessing. These silver halide fine grains are preferably not fogged inadvance. In the fine grain silver halide, the content of silver bromideis any of 0 to 100 mole %. The fine grain-silver halide may containsilver chloride and/or silver iodide, if necessary. The fine grainsilver halide preferably contains silver iodide of 0.5 to 10 mol %. Theaverage grain diameter (the average value of a diameter of a circlewhose area is equivalent to the projected area of an individual grain)of the fine grain silver halide is preferably 0.01 to 0.5 μm, morepreferably 0.02 to 0.2 μm.

The fine grain silver halide may be prepared following the sameprocedure as for a conventional light-sensitive silver halide grains.The surface of each silver halide grain need not be optically sensitizednor spectrally sensitized. However, before the silver halide grains areadded to a coating solution, it is preferable to add known stabilizers,such as triazole-series compounds, azaindene-series compounds,benzothiazolium-series compounds, mercapto-series compounds and zinccompounds. Colloidal silver may be added to this fine grain silverhalide grains-containing layer.

The coating amount of silver in the light-sensitive material of thepresent invention, preferably of the first embodiment, is preferably 6.0g/m² or less, and most preferably 4.5 g/m² or less.

The photographic additives that can be used in the present invention,preferably in the first embodiment, are described in RDs, whoseparticular parts are given below in the following table. Kind ofAdditive RD 17643 RD 18716 RD 307105 1. Chemical p.23 p.648 (right p.866sensitizers column) 2. Sensitivity- — p.648 (right — enhancing column)agents 3. Spectral pp.23-24 pp.648 (right pp.866-868 sensitizers andcolumn)-649 Supersensitizers (right column) 4. Brightening p.24 pp.647(right p.868 agents column) 5. Light pp.25-26 pp.649 (right p.873absorbers, column)-650 Filters, Dyes, (left column) and UV Absorbers 6.Binders p.26 p.651 (left pp.873-874 column) 7. Plasticizers p.27 p.650(right p.876 and Lubricants column) 8. Coating aids pp.26-27 p.650(right pp.875-876 and Surfactants column) 9. Antistatic p.27 p.650(right pp.876-877 agents column) 10. Matting agents — — pp.878-879

In the light-sensitive material of the present invention, preferably ofthe first embodiment, various dye-forming couplers may be used incombination with the coupler for use in the present invention. Thefollowing couplers are especially preferred.

Yellow coupler (which may be used in combination with the couplerrepresented by formula (I)): a coupler represented by formula (I) or(II) in EP 502,424A; a coupler represented by formula (I) or (2) in EP513,496A (especially, Y-28 on page 18); a coupler represented by formula(I) in claim 1 in EP 568,037A; a coupler represented by formula (I) inlines 45 to 55 in column 1 in U.S. Pat. No. 5,066,576; a couplerrepresented by formula (I) in paragraph 0008 in JP-A-4-274425; a couplerdescribed in claim 1 on page 40 in EP 498,381A1 (especially, D-35 onpage 18); a coupler represented by formula (Y) on page 4 in EP 447,969A1(especially, Y-1 on page 17, Y-54 on page 41); a coupler represented byformula (II) to (IV) in lines 36 to 58 in column 7 in U.S. Pat. No.4,476,219 (especially, II-17, 19 (column 17), II-24 (column 19)).

Magenta coupler: L-57 (page 11, right and lower column), L-68 (page 12,right and lower column), L-77 (page 13, right and lower column) inJP-A-3-39737; [A-4]-63 (page 134), [A-4]-73, -75 (page 139) in EP456,257; M-4, -6 (page 26), M-7 (page 27) in EP 486,965; M-45 (page 19)in EP 571,959A; (M-1) (page 6) in JP-A-5-204106; M-22 in paragraph[0237] in JP-A-4-362631.

Cyan coupler: CX-1, 3, 4, 5, 11, 12, 14, 15 (pages 14 to 16) inJP-A-4-204843; C-7, 10 (page 35), 34, 35 (page 37), (1-1), (1-17) (pages42 to 43) in JP-A-4-43345; a coupler represented by formula (Ia) or (Ib)in claim 1 in JP-A-6-67385.

Polymer coupler: P-1, P-5 (page 11) in JP-A-2-44345.

Preferable examples of couplers, which form a color dye having asuitable diffusive property, include those described in U.S. Pat. No.4,366,237, GB 2,125,570, EP 96,873B, and DE 3,234,533.

Preferable examples of the coupler, which is used for compensatingunnecessary absorption of a color dye, include a yellow-colored cyancoupler represented by formulae (CI), (CII), (CIII), and (CIV) describedon page 5 in EP 456,257A1 (especially, YC-86 on page 84), ayellow-colored magenta coupler, ExM-7 (page 202), EX-1 (page 249), EX-7(page 251), described in EP 456,257A1, a magenta-colored cyan coupler,CC-9 (column 8), CC-13 (column 10), described in U.S. Pat. No.4,833,069, and a colorless masking coupler, represented by Formula (2)(column 8) in Us 4,837,136, and formula (A) in claim 1 in WO92/11575(particularly the exemplified compounds on pages 36 to 45).

Examples of the compound (including a coupler), which reacts with anoxidized product of a developing agent, to release a photographicallyuseful compound's residue, include the followings:

Development inhibitor releasing compounds: compounds represented by anyone of Formulae (I), (II), (III), and (IV) described on page 11 in EP378,236A1, (especially, T-101 (page 30), T-104 (page 31), T-113 (page36), T-131 (page 45), T-144 (page 51), T-158 (page 58)); compoundsrepresented by Formula (I) described on page 7 in EP 436,938A2,(especially, (D-49) (page 51); compounds represented by Formula (1) inEP 568,037A (especially, (23) (page 11), and compounds represented byFormula (I), (II), or (III) described on pages 5 to 6 in EP440,195A2,(especially, 1-(1) on page 29).

Bleaching accelerator releasing compounds: compounds represented byFormula (I) or (I′) described on page 5 in EP 310,125A2, (especially,(60), (61) on page 61) and compounds represented by Formula (I)described in claim 1 of JP-A-6-59411, (especially, (7) on page 7).

Ligand releasing compounds: compounds represented by LIG-X described inclaim 1 of U.S. Pat. No. 4,555,478, (especially, a compound in lines 21to 41 in column 12).

Leuco dye releasing compounds: compounds 1 to 6 in U.S. Pat. No.4,749,641, columns 3 to 8; Fluorescent dye releasing compounds:compounds represented by COUP-DYE described in claim 1 of U.S. Pat. No.4,774,181, (especially, compounds 1 to 11 in column 7 to 10).

Compounds, which release a development accelerator or a fogging agent:compounds represented by Formula (1), (2) or (3) in U.S. Pat. No.4,656,123, column 3, (especially, (1-22) in column 25), and the compoundExZK-2 described on page 75, lines 36 to 38, in EP 450,637A2.

Compounds which release a group capable of becoming a dye only afterbeing split-off: compounds represented by Formula (1) described in claim1 of U.S. Pat. No. 4,857,447, (especially, Y-1 to Y-19 in column 25 to36).

As additives other than the coupler, the following ones are preferable.

Dispersion media for an oil-soluble organic compound: P-3, 5, 16, 19,25, 30, 42, 49, 54, 55, 66, 81, 85, 86 and 93 (page 140 to page 144) inJP-A-62-215272; latex for impregnation with the oil-soluble organiccompound: latex described in U.S. Pat. No. 4,199,363; scavengers for anoxidized product of a developing agent: compounds represented by theformula (I) in U.S. Pat. No. 4,978,606, column 2, line 54 to line 62(particularly I-, (1), (2), (6), (12) (columns 4 to 5)), and compoundsrepresented by the formula in U.S. Pat. No. 4,923,787, column 2, line 5to line 10 (particularly Compound 1 (column 3)); stain preventiveagents: compounds represented by one of the formulae (1) to (III) in EP298321A, page 4, line 30 to line 33 (particularly, I-47, 72, III-1, 27(page 24 to page 48)); anti-fading agents: A-6, 7, 20, 21, 23, 24, 25,26, 30, 37, 40, 42, 48, 63, 90, 92, 94 and 164 (page 69 to page 118) inEP 298321A, and II-1 to III-23 in U.S. Pat. No. 5,122,444, columns 25 to38 (particularly, III-10), I-1 to III-4 in EP 471347A, page 8 to page 12(particularly, II-2), and A-1 to 48 in U.S. Pat. No. 5,139,931, columns32 to 40 (particularly A-39 and 42); materials reducing the amount of acolor development-enchanting agent or a color contamination preventiveagent to be used: I-1 to II-15 in EP 411324A, page 5 to page 24(particularly, I-46); formalin scavengers: SCV-1 to 28 in EP 477932A,page 24 to page 29 (particularly SCV-8); hardener: H-1, 4, 6, 8 and 14in JP-A-1-214845 in page 17, compounds (H-1 to H-54) represented by oneof the formulae (VII) to (XII) in U.S. Pat. No. 4,618,573, columns 13 to23, compounds (H-1 to 76) represented by the formula (6) inJP-A-2-214852, page 8, the lower right (particularly, H-14), andcompounds described in claim 1 in U.S. Pat. No. 3,325,287; precursors ofdeveloping inhibitor: P-24, 37, 39 (page 6 to page 7) in JP-A-62-168139,and compounds described in claim 1 of U.S. Pat. No. 5,019,492(particularly 28 to 29 in column 7); antiseptics and mildew-proofingagents: I-1 to III-43 in U.S. Pat. No. 4,923,790, columns 3 to 15(particularly II-1, 9, 10 and 18 and III-25); stabilizers andantifoggants: I-1 to (14) in U.S. Pat. No. 4,923,793, columns 6 to 16(particularly, I-1, 60, (2) and (13)) and compounds 1 to 65 in U.S. Pat.No. 4,952,483, columns 25 to 32 (particularly, 36); chemicalsensitizers: triphenylphosphine selenide, and compound 50 inJP-A-5-40324; dyes: a-1 to b-20 in JP-A-3-156450, page 15 to page 18(particularly, a-1, 12, 18, 27, 35, 36, b-5 and V-1 to 23 on pages 27 to29, particularly, V-1), F-1-1 to F-II-43 in EP 445627A, page 33 to page55 (particularly F-I-11 and F-II-8), III-1 to 36 in EP 457153A, page 17to page 28 (particularly III-1 and 3), microcrystal dispersions of Dye-1to 124 in WO88/04794, 8 to 26, compounds 1 to 22 in EP319999A, page 6 topage 11 (particularly, compound 1), compounds D-1 to 87 (page 3 to page2-8) represented by one of the formulae (1) to (3) in EP 519306A,compounds 1 to 22 (columns 3 to 10) represented by the formula (I) inU.S. Pat. No. 4,268,622, compounds (I) to (31) (columns 2 to 9)represented by the formula (I) in U.S. Pat. No. 4,923,788; UV absorbers:compounds (18b) to (18r) and 101 to 427 (page 6 to page 9) representedby the formula (I) in JP-A-46-3335, compounds (3) to (66) (page 10 topage 44) represented by the formula (I) and compounds HBT-1 to HBT-10(page 14) represented by the formula (III) in EP 520938A, and compounds(I) to (31) (columns 2 to 9) represented by the formula (I) in EP521823A.

The present invention, preferably the first embodiment can be applied tovarious color light-sensitive materials, such as black-and-whiteprinting papers, black-and-white negative films, X-ray films, colornegative films for general purposes or movies, color reversal films forslides or television, color papers, color positive films, and colorreversal papers. Additionally, the present invention, preferably thefirst embodiment can be preferably applied to a film unit with a lens,as described in JP-B-2-32615 or JU-B-3-39784 (“JU-B” means an examinedJapanese Utility model registration publication).

A support that can be suitably used in the present invention, preferablyin the first embodiment, is described in, for example, theabove-described R.D. No. 17643 (page 28), R.D. No. 18716 (page 647,right column to page 648, left column) and R.D. No. 307105 (page 879).

In a light-sensitive material of the present invention, preferably ofthe first embodiment, the total film thickness of hydrophilic colloidlayers on the side having silver halide emulsion layers is preferably 28μm or less, more preferably 23 μm or less, still more preferably 18 μmor less, and particularly preferably 16 μm or less. A film swellingspeed T_(1/2) is preferably 30 sec or less, and more preferably 20 secor less. T_(1/2) is defined as a time required to reach ½ the saturatedfilm thickness, which is 90% of the maximum swelled film thicknessreached when the film is processed with a color developer at 30° C. for3 min and 15 sec. The film thickness means the thickness of a filmmeasured under controlled moisture condition, at a temperature of 25° C.and a relative humidity of 55% (two days). T_(1/2) can be measured byusing a swellometer of a type described in Photogr. Sci. Eng., by A.Green et al., Vol. 19, 2, pp. 124 to 129. T_(1/2) can be adjusted addinga film hardener to gelatin as a binder, or changing aging conditionsafter coating. The swell ratio is preferably 150 to 400%. The swellratio can be calculated from the maximum swollen film thickness underthe conditions above by using the expression: (maximum swollen filmthickness−film thickness)/film thickness.

In the light-sensitive material of the present invention, preferably thefirst embodiment, hydrophilic colloid layers (referred to as backinglayers) having a total dried film thickness of 2 to 20 μm are preferablyformed, on the side opposite to the side having emulsion layers. Thebacking layers preferably contain, the aforementioned light absorbents,filter dyes, ultraviolet absorbents, antistatic agents, film hardeners,binders, plasticizers, lubricants, coating aids, and surfactants. Theswell ratio of the backing layer is preferably 150 to 500%.

The light-sensitive materials of the present invention, preferably thefirst embodiment can be subjected to development processing according tousual manner, as described in the above-mentioned R.D. No. 17643, pp. 28to 29, R.D. No. 18716, page 651, left to right columns, and R.D. No.307105, pp. 880 to 881.

Next, color negative film processing solutions for use in the presentinvention, preferably the first embodiment will be described below.

Compounds described in JP-A-4-121739, from page 9, upper right column,line 1, to page 11, lower left column, line 4, can be used in a colordeveloper that can be used in the present invention, preferably in thefirst embodiment. As a color-developing agent used when particularlyrapid processing is to be performed,2-methyl-4-[N-ethyl-N-(2-hydroxyethyl)amino]aniline,2-methyl-4-[N-ethyl-N-(3-hydroxypropyl)amino]aniline, and2-methyl-4-[N-ethyl-N-(4-hydroxybutyl)amino]aniline are preferable.

The amount to be used of any of these color-developing agents ispreferably 0.01 to 0.08 mole, more preferably 0.015 to 0.06 mole, andespecially preferably 0.02 to 0.05 mole, per liter of a color developer.Also, a replenisher of a color developer preferably contains acolor-developing agent at a concentration 1.1 to 3 times, particularlypreferably 1.3 to 2.5 times the above concentration.

As a preservative of a color developer, hydroxylamine can be extensivelyused. When higher preservability is necessary, the use of ahydroxylamine derivative having a substituent such as an alkyl group, ahydroxyalkyl group, a sulfoalkyl group, or a carboxyalkyl group ispreferable. Preferable examples includeN,N-di-(sulfoethyl)hydroxylamine, monomethylhydroxylamine,dimethylhydroxylamine, monoethylhydroxylamine, diethylhydroxylamine, andN,N-di(carboxylethyl)hydroxylamine. Of these derivatives,N,N-di-(sulfoethyl)hydroxylamine is particularly preferable. Althoughthese derivatives can be used together with hydroxylamine, it ispreferable to use one or two types of these derivatives instead ofhydroxylamine.

The amount to be used of a preservative is preferably 0.02 to 0.2 mole,more preferably 0.03 to 0.15 mole, and especially preferably 0.04 to 0.1mole per liter. As in the case of a color-developing agent, areplenisher preferably contains a preservative at a concentration 1.1 to3 times the concentration of a mother solution (processing tanksolution).

A color developer contains sulfite as an agent for preventing an oxideof a color-developing agent from changing into tar. The amount to beused of this sulfite is preferably 0.01 to 0.05 mole, more preferably0.02 to 0.04 mole per liter. Sulfite is preferably used in a replenisherat a concentration 1.1 to 3 times the above concentration.

The pH of a color developer is preferably 9.8 to 11.0, and morepreferably 10.0 to 10.5. In a replenisher, the pH is preferably set tobe higher by 0.1 to 1.0 than the above values. To stably maintain such apH, a known buffer agent such as carbonate, phosphate, sulfosalicylate,or borate is used.

The replenishment rate of a color developer is preferably 80 to 1,300 mlper m² of a light-sensitive material to be processed. The replenishmentrate is preferably smaller in order to reduceenvironmental-pollution-load. For example, the replenishment rate ispreferably 80 to 600 ml, and more preferably 80 to 400 ml.

The bromide ion concentration in a color developer is usually 0.01 to0.06 mole per liter. This bromide ion concentration is preferably set at0.015 to 0.03 mole per liter, for the purpose of suppressing fog toimprove discrimination with maintaining sensitivity, and of improvinggraininess at the same time. To set the bromide ion concentration inthis range, it is only necessary to add bromide ion calculated by thefollowing equation, to a replenisher. When C takes a negative value,however, no bromide ions are preferably added to a replenisher.C=(A−W)/Vin whichC: a bromide ion concentration (mole/L) in a color developer replenisherA: a target bromide ion concentration (mole/L) in a color developerW: an amount (mole) of bromide ions dissolving into a color developerfrom a light-sensitive material when 1 m² of the light-sensitivematerial is color-developedV: a replenishment rate (L) of a color developer replenisher to 1 m² ofa light-sensitive material

As a method of increasing the sensitivity when the replenishment rate isdecreased or high bromide ion concentration is set, it is preferable touse a development accelerator such as pyrazolidones represented by1-phenyl-3-pyrazolidone, and1-phenyl-2-methyl-2-hydroxymethyl-3-pyrazolidone, or a thioethercompound represented by 3,6-dithia-1,8-octanediol.

Compounds and processing conditions described in JP-A-4-125558, frompage 4, lower left column, line 16, to page 7, lower left column, line6, can be applied to a processing solution having a bleaching capacityin the present invention, preferably in the first embodiment.

The bleaching agent preferably has an oxidation-reduction potential of150 mV or more. Preferable specific examples of the bleaching agent aredescribed in JP-A-5-72694 and JP-A-5-173312. In particular,1,3-diaminopropane tetraacetic acid and ferric complex salt of acompound shown as specific example 1 in JP-A-5-173312, page 7, arepreferable.

Further, to improve the biodegradability of a bleaching agent, it ispreferable to use ferric complex salt of a compound described inJP-A-4-251845, JP-A-4-268552, EP 588,289, EP 591,934 and JP-A-6-208213,as a bleaching agent. The concentration of any of these bleaching agentsis preferably 0.05 to 0.3 mole per liter of a solution having ableaching capacity. To reduce the amount of discharge to theenvironment, the concentration is preferably designed to be 0.1 to 0.15mole per liter of the solution having a bleaching capacity. When thesolution having a bleaching capacity is a bleaching solution, preferably0.2 to 1 mole, and more preferably 0.3 to 0.8 mole of a bromide is addedper liter.

A replenisher of the solution having a bleaching capacity basicallycontains components at concentrations calculated by the followingequation. This makes it possible to maintain the concentrations in amother solution constant.C _(R) ═C _(T) X(V ₁ +V ₂)/V ₁ +C _(P)In which

-   -   C_(R): concentration of a component in a replenisher    -   C_(T): concentration of a component in a mother solution        (processing tank solution)    -   C_(P): concentration of a component consumed during processing    -   V₁: a replenishment rate (ml) of a replenisher having a        bleaching capacity per m² of a light-sensitive material    -   V2: an amount (ml) of carryover from a preceding bath by m² of a        light-sensitive material

Additionally, a bleaching solution preferably contains a pH bufferingagent, and particularly preferably, it contains a dicarboxylic acid withlittle odor, such as succinic acid, maleic acid, malonic acid, glutaricacid, and adipic acid. Also, the use of known bleaching acceleratorsdescribed in JP-A-53-95630, RD No. 17129, and U.S. Pat. No. 3,893,858 ispreferable.

It is preferable to replenish 50 to 1,000 ml of a bleaching replenisherto a bleaching solution, per m² of a light-sensitive material. Thereplenishment rate is more preferably 80 to 500 ml, and especiallypreferably 100 to 300 ml. Conducting aeration of a bleaching solution isalso preferable.

Compounds and processing conditions described in JP-A-4-125558, frompage 7, lower left column, line 10, to page 8, lower right column, line19, can be applied to a processing solution with a fixing capacity. Inparticular, to improve the fixing speed and preservability, the compoundrepresented by formulae (1) or (II) described in JP-A-6-301169 ispreferably added singly or in combination, a processing solution with afixing capacity. To improve preservability, the use of sulfinic acid,including p-toluenesulfinate, described in JP-A-1-224762 is alsopreferable.

To improve the desilvering characteristics, ammonium is preferably usedas cation, in a processing solution with a bleaching capacity or aprocessing solution with a fixing capacity. However, the amount ofammonium is preferably reduced, or not used at all, to reduceenvironmental pollution. In the bleaching, bleach-fixing, and fixingsteps, it is particularly preferable to perform jet stirring describedin JP-A-1-309059.

The replenishment rate of a replenisher in the bleach-fixing, or fixingstep is preferably 100 to 1,000 ml, more preferably 150 to 700 ml, andfurthermore preferably 200 to 600 ml per m² of a light-sensitivematerial.

In the bleach-fixing, or fixing step, an appropriate silver collectingapparatus is preferably installed either in-line or off-line to collectsilver. When such an apparatus is installed in-line, processing can beperformed while the silver concentration in a solution is reduced, andas a result of this, the replenishment rate can be reduced. It is alsopreferable to install such an apparatus off-line to collect silver andreuse the residual solution as a replenisher.

The bleach-fixing, or fixing step can be performed using a plurality ofprocessing tanks, and these tanks are preferably piped in a cascademanner to form a multistage counter flow system. To balance the size ofa processor, two-tank cascade system is generally efficient. Theprocessing time ratio of the preceding tank to the subsequent tank ispreferably (0.5:1) to (1:0.5), and more preferably (0.8:1) to (1:0.8).

In a bleach-fixing, or fixing solution, the presence of a free chelatingagent, which is not a metal complex, is preferable to improve thepreservability. As these chelating agents, the use of the biodegradablechelating agents previously described in connection to a bleachingsolution is preferable.

Contents described in aforementioned JP-A-4-125558, from page 12, lowerright column, line 6, to page 13, lower right column, line 16, can beapplied to the washing and stabilization steps. To improve the safety ofthe working environment, it is preferable to use azolylmethylaminesdescribed in EP 504,609 and EP 519,190 or N-methylolazoles described inJP-A-4-362943, instead of formaldehyde, in a stabilizer, and to make amagenta coupler two-equivalent so that a solution of surfactantcontaining no image stabilizing agent such as formaldehyde can be used.

To reduce adhesion of dust to a magnetic recording layer coated on alight-sensitive material, a stabilizer described in JP-A-6-289559 can bepreferably used.

The replenishment rate of washing water and a stabilizer is preferably80 to 1,000 ml, more preferably 100 to 500 ml, and especially preferably150 to 300 ml, per m² of a light-sensitive material to be processed, tomaintain the washing and stabilization functions and at the same timereduce the waste liquors for environmental conservation. In a processingperformed with such a replenishment rate, it is preferable to preventthe propagation of bacteria and mildew by using known mildew-proofingagents such as thiabendazole, 1,2-methylisothiazoline-3-one, and5-chloro-2-methylisothiazoline-3-one, antibiotics such as gentamicin,and water deionized by an ion exchange resin or the like. It is moreeffective to use deionized water together with a mildew-proofing agentor an antibiotic.

The replenishment rate of a solution in a washing water tank orstabilizer tank is preferably reduced by a reverse osmosis membranetreatment described in JP-A-3-46652, JP-A-3-53246, JP-A-355542,JP-A-3-121448, and JP-A-3-126030. A reverse osmosis membrane used inthis treatment is preferably a low-pressure reverse osmosis membrane.

In the processing that is used in the present invention, preferably inthe first embodiment, it is particularly preferable to performevaporation correction of the processing solution as described in JIIIJournal of Technical Disclosure No. 94-4992. In particular, a method ofperforming correction on the basis of (formula-1) on page 2, by usingtemperature and humidity information of an environment in which aprocessor is set is preferable. Water for use in this evaporationcorrection is preferably taken from the washing water replenishmenttank. If this is the case, deionized water is preferably used as thewashing replenishing water.

Processing agents described in aforementioned JIII Journal of TechnicalDisclosure No. 94-4992, from page 3, right column, line 15, to page 4,left column, line 32, are preferably used in the present invention,preferably in the first embodiment. As a processor used with theseprocessing agents, a film processor described on page 3, right column,lines 22 to 28, is preferable.

Specific examples of processing agents, automatic processors, andevaporation correction methods suited to practicing the presentinvention, preferably the first embodiment are described inaforementioned JIII Journal of Technical Disclosure No. 94-4992, frompage 5, right column, line 11, to page 7, right column, last line.

Processing agents used in the present invention, preferably in the firstembodiment can be supplied in any form such as a liquid agent having theconcentration as it is to be used, a concentrated liquid agent,granules, powder, tablets, paste, and emulsion. Examples of suchprocessing agents are a liquid agent contained in a low-oxygen permeablevessel as described in JP-A-63-17453, vacuum-packed powders and granulesdescribed in JP-A-4-19655 and JP-A-4-230748, granules containing awater-soluble polymer described in JP-A-4-221951, tablets described inJP-A-51-61837 and JP-A-6-102628, and a paste described inJP-T-57-500485. Although any of these processing agents can bepreferably used, the use of a liquid adjusted to have the concentrationas it is to be used, in advance, is preferable for the sake ofconvenience in use.

As a vessel for containing these processing agents, polyethylene,polypropylene, polyvinylchloride, polyethyleneterephthalate, nylon andthe like, are used singly or as a composite material. These materialsare selected in accordance with the level of necessary oxygenpermeability. For a readily oxidizable solution such as a colordeveloper, a low oxygen permeable material is preferable. Morespecifically, polyethyleneterephthalate or a composite material ofpolyethylene and nylon is preferable. A vessel made of any of thesematerials preferably has a thickness of 500 to 1,500 μm and ispreferably adjusted to have oxygen permeability of 20 ml/m²·24 ·hrs atomor less.

Next, color reversal film processing solution used in the presentinvention, preferably in the first embodiment will be described below.

Processing for a color reversal film is described in detail in AztechLtd., Kochi Gijutsu No. 6 (1991, April 1), from page 1, line 5, to page10, line 5, and from page 15, line 8, to page 24, line 2, and any of thecontents can be preferably applied.

In a color reversal film processing, an image-stabilizing agent iscontained in a control bath or a final bath. Preferable examples of suchan image-stabilizing agent are formalin, sodium formaldehyde-bisulfite,and N-methylolazoles. Sodium formaldehyde-bisulfite, andN-methylolazoles are preferable in terms of preserving workingenvironment, and N-methyloltriazole is particularly preferable asN-methylolazoles. The contents pertaining to a color developer,bleaching solution, fixing solution, and washing water described in thecolor negative film processing can be preferably applied to the colorreversal film processing.

Preferable examples of color reversal film processing agents containingthe above contents are an E-6 processing agent manufactured by EastmanKodak Co. and a CR-56 processing agent manufactured by Fuji Photo FilmCo., Ltd.

Next, a magnetic recording layer preferably used in the presentinvention, preferably in the first embodiment is explained.

The magnetic recording layer preferably used in the present invention,preferably in the first embodiment refers to a layer provided by coatinga base with an aqueous or organic solvent coating solution containingmagnetic particles dispersed in a binder.

To prepare the magnetic particles used in the present invention,preferably in the first embodiment, use can be made of a ferromagneticiron oxide such as γFe₂O₃, Co-coated γFe₂O₃, Co-coated magnetite,Co-containing magnetite, ferromagnetic chromium dioxide, a ferromagneticmetal, a ferromagnetic alloy, hexagonal Ba ferrite, Sr ferrite, Pbferrite, Ca ferrite, and the like. A Co-coated ferromagnetic iron oxide,such as Co-coated γFe₂O₃, is preferable. The shape may be any of aneedle shape, a rice grain shape, a spherical shape, a cubic shape, atabular shape, and the like. The specific surface area is preferably 20m²/g or more, and particularly preferably 30 m²/g or more, in terms ofS_(BET).

The saturation magnetization (as) of the ferromagnetic material ispreferably 3.0×10⁴ to 3.0×10⁵ A/m, and particularly preferably 4.0×10⁴to 2.5×10⁵ A/m. The ferromagnetic particles may be surface-treated withsilica and/or alumina or an organic material. The surface of themagnetic particles may be treated with a silane coupling agent or atitanium coupling agent, as described in JP-A-6-161032. Further,magnetic particles whose surface is coated with an inorganic or organicmaterial, as described in JP-A-4-259911 and JP-A-5-81652, can be used.

As the binder that can be used for the magnetic particles, as describedin JP-A-4-219569, a thermoplastic resin, a thermosetting resin, aradiation-setting resin, a reactive resin, an acid-degradable polymer,an alkali-degradable polymer, a biodegradable polymer, a natural polymer(e.g. a cellulose derivative and a saccharide derivative), and a mixtureof these can be used. The above resins have a Tg of −40 to 300° C. and aweight-average molecular weight of 2,000 to 1,000,000. Examples includevinyl copolymers, cellulose derivatives, such as cellulose diacetates,cellulose triacetates, cellulose acetate propionates, cellulose acetatebutylates, and cellulose tripropionates; acrylic resins, and polyvinylacetal resins. Gelatin is also preferable. Cellulose di(tri)acetates areparticularly preferable. To the binder may be added an epoxy, aziridine,or isocyanate crosslinking agent, to harden the binder. Examples of theisocyanate crosslinking agent include isocyanates, such as tolylenediisocyanate, 4,4′-diphenylmethane diisocyanate, hexamethylenediisocyanate, and xylylene diisocyanate; reaction products of theseisocyanates with polyalcohols (e.g. a reaction product of 3 mol oftolylene diisocyanate with 1 mol of trimethylolpropane), andpolyisocyanates produced by condensation of these isocyanates. Those aredescribed, for example, in JP-A-6-59357.

The method of dispersing the foregoing magnetic material in theforegoing binder is preferably one described in JP-A-6-35092, in whichmethod use is made of a kneader, a pin-type mill, an annular-type mill,and the like, which may be used alone or in combination. A dispersantdescribed in JP-A-5-088283 and other known dispersants can be used. Thethickness of the magnetic recording layer is generally 0.1 to 10 μm,preferably 0.2 to 5 μm, and more preferably 0.3 to 3 μm. The weightratio of the magnetic particles to the binder is preferably from(0.5:100) to (60:100), and more preferably from (1:100) to (30:100). Thecoating amount of the magnetic particles is generally 0.005 to 3 g/m²,preferably 0.01 to 2 g/m², and more preferably 0.02 to 0.5 g/m². Thetransmission yellow density of the magnetic recording layer ispreferably 0.01 to 0.50, more preferably 0.03 to 0.20, and particularlypreferably 0.04 to 0.15. The magnetic recording layer can be provided tothe undersurface of the photographic base by coating or printing throughall parts or in a striped fashion. To apply the magnetic recordinglayer, use can be made of an air doctor, blade, air knife, squeezing,impregnation, reverse roll, transfer roll, gravure, kiss, cast,spraying, dipping, bar, extrusion, or the like. A coating solutiondescribed, for example, in JP-A-5-341436 is preferable.

The magnetic recording layer may be provided with functions, forexample, of improving lubricity, of regulating curling, of preventingelectrification, of preventing adhesion, and of abrading a head, or itmay be provided with another functional layer that is provided withthese functions. An abrasive in which at least one type of particlescomprises aspherical inorganic particles having a Mohs hardness of 5 ormore, is preferable. The aspherical inorganic particles preferablycomprise a fine powder of an oxide, such as aluminum oxide, chromiumoxide, silicon dioxide, and titanium dioxide; a carbide, such as siliconcarbide and titanium carbide; diamond, or the like. The surface of theseabrasives may be treated with a silane coupling agent or a titaniumcoupling agent. These particles may be added to the magnetic recordinglayer, or they may form an overcoat (e.g. a protective layer and alubricant layer) on the magnetic recording layer. As a binder that canbe used at that time, the above-mentioned binders can be used, andpreferably the same binder as mentioned for the magnetic recording layeris used. Light-sensitive materials having a magnetic recording layer aredescribed in U.S. Pat. Nos. 5,336,589, 5,250,404, 5,229,259, and5,215,874, and European Patent No. 466,130.

A polyester support that is preferably used in the present invention,preferably in the first embodiment will be described below. Details ofthe polyester support, as well as details of light-sensitive materials,processing, cartridges, and examples (to be described later), aredescribed in JIII Journal of Technical Disclosure No. 94-6023 (JapanInstitute of Invention & Innovation, Mar. 15, 1994). Polyester for usein the present invention, preferably in the first embodiment is formedfrom diol and aromatic dicarboxylic acid as essential components.Examples of the aromatic dicarboxylic acid are 2,6-, 1,5-, 1,4-, and2,7-naphthalene dicarboxylic acids, terephthalic acid, isophthalic acid,and phthalic acid. Examples of the diol are diethyleneglycol,triethyleneglycol, cyclohexanedimethanol, bisphenol A, and bisphenol.Examples of the polymer are homopolymers such aspolyethyleneterephthalate, and polyethylenenaphthalate, andpolycyclohexanedimethanol terephthalate. Polyester containing 50 to 100mole % of 2,6-naphthalenedicarboxylic acid is particularly preferable.Polyethylene-2,6-naphthalate is particularly preferable among the abovepolymers. The average molecular weight is generally in the range ofabout 5,000 and 200,000. The Tg of the polyester for use in the presentinvention, preferably in the first embodiment is generally 50° C. orhigher, preferably 90° C. or higher.

The polyester base is heat-treated at a heat treatment temperature ofgenerally 40° C. or over, but less than the Tg, and preferably at a heattreatment temperature of the Tg −20° C. or more, but less than the Tg,so that it will hardly have core set curl. The heat treatment may becarried out at a constant temperature in the above temperature range, orit may be carried out with cooling. The heat treatment time is generally0.1 hours or more, but 1,500 hours or less, and preferably 0.5 hours ormore, but 200 hours or less. The heat treatment of the base may becarried out with the base rolled, or it may be carried out with it beingconveyed in the form of web. The surface of the base may be made rough(unevenness, for example, by applying electroconductive inorganicfine-particles, such as SnO₂ and Sb₂O₅), so that the surface state maybe improved. Further, it is desirable to provide, for example, arollette (knurling) at the both ends for the width of the base (bothright and left ends towards the direction of rolling) to increase thethickness only at the ends, so that a trouble of deformation of the basewill be prevented. The trouble of deformation of the support means that,when a support is wound on a core, on its second and further windings,the support follows unevenness of its cut edge of the first winding,deforming its flat film-shape. These heat treatments may be carried outat any stage after the production of the base film, after the surfacetreatment, after the coating of a backing layer (e.g. with an antistaticagent and a slipping agent), and after coating of an undercoat, withpreference given to after coating of an antistatic agent.

Into the polyester may be blended (kneaded) an ultraviolet absorber.Further, prevention of light piping can be attained by blending dyes orpigments commercially available for polyesters, such as Diaresin (tradename, manufactured by Mitsubisi Chemical Industries Ltd.), and Kayaset(trade name, manufactured by Nippon Kayaku Co., Ltd.).

In the present invention, preferably in the first embodiment, thesesupports are preferably subjected to a surface treatment, in order toachieve strong adhesion between the support and a photographicconstituting layer. For the above-mentioned surface treatment, varioussurface-activation treatments can be used, such as a chemical treatment,a mechanical treatment, a corona discharge treatment, a flame treatment,an ultraviolet ray treatment, a high-frequency treatment, a glowdischarge treatment, an active plasma treatment, a laser treatment, amixed acid treatment, and an ozone oxidation treatment. Among thesurface treatments, an ultraviolet irradiation treatment, a flametreatment, a corona treatment, and a glow treatment are preferable.

With respect to the undercoating, a single layer or two or more layersmay be used. As the binder for the undercoat layer, for example,copolymers produced by using, as a starting material, a monomer selectedfrom among vinyl chloride, vinylidene chloride, butadiene, methacrylicacid, acrylic acid, itaconic acid, maleic anhydride, and the like, aswell as polyethylene imines, epoxy resins, grafted gelatins,nitrocelluloses, and gelatins, can be mentioned. As compounds that canswell the base, resorcin and p-chlorophenol can be mentioned. As gelatinhardening agents in the undercoat layer, chrome salts (e.g. chromealum), aldehydes (e.g. formaldehyde and glutaraldehyde), isocyanates,active halogen compounds (e.g. 2,4-dichloro-6-hydroxy-s-triazine),epichlorohydrin resins, active vinyl sulfone compounds, and the like canbe mentioned. SiO₂, TiO₂, inorganic fine particles, or polymethylmethacrylate copolymer fine particles (0.01 to 10 μm) may be included asa matting agent.

Further, in the present invention, preferably in the first embodiment,an antistatic agent is preferably used. As the antistatic agent,polymers containing a carboxylic acid, a carboxylate, or a sulfonate;cationic polymers, and ionic surface-active compounds can be mentioned.Most preferable antistatic agents are fine particles of at least onecrystalline metal oxide selected from the group consisting of ZnO, TiO₂,SnO₂, Al₂O₃, In₂O₃, SiO₂, MgO, BaO, MoO₃, and V₂O₅, and having aspecific volume resistivity of 10⁷ Ωcm or less, and more preferably 10⁵Ωcm or less and a particle size of 0.001 to 1.0 μm, or fine particles oftheir composite oxides (Sb, P, B, In, S, Si, C, and the like); as wellas fine particles of the above metal oxides in the form of a sol, orfine particles of composite oxides of these. The content thereof in thelight-sensitive material is preferably 5 to 500 mg/m², and particularlypreferably 10 to 350 mg/m². The ratio of the amount of theelectroconductive crystalline oxide or its composite oxide to the amountof the binder is preferably from 1/300 to 100/1, and more preferablyfrom 1/100 to 100/5.

The light-sensitive material of the present invention, preferably of thefirst embodiment preferably has a slip property. Slip agent-containinglayers are preferably formed on both the sides of alight-sensitive-layer side and a back-layer side. A preferable slipproperty is 0.01 to 0.25 as a coefficient of kinetic friction. Thisrepresents a value obtained when a sample is transferred againststainless steel sphere of 5 mm in diameter, at a speed of 60 cm/min (25°C., 60% RH). In this evaluation, a value of nearly the same level isobtained when the surface of a light-sensitive layer is used as apartner material in place of the stainless steel sphere.

Examples of a slip agent that can be used in the present invention,preferably in the first embodiment include polyorganosiloxane, higherfatty acid amide, higher fatty acid metal salt, and ester of higherfatty acid and higher alcohol. As the polyorganosiloxane, it is possibleto use, e.g., polydimethylsiloxane, polydiethylsiloxane,polystyrylmethylsiloxane, or polymethylphenylsiloxane. A layer to whichthe slip agent is added is preferably the outermost emulsion layer or abacking layer. Polydimethylsiloxane and ester having a long-chain alkylgroup are particularly preferable.

The light-sensitive material of the present invention, preferably of thefirst embodiment preferably contains a matting agent. This matting agentcan be added to either the emulsion side or back side, and especiallypreferably added to the outermost layer of the emulsion layer side. Thematting agent can be either soluble or insoluble in processing solution,and the use of both types of matting agents is preferable. Preferableexamples are polymethylmethacrylate grains, poly(methylmethacrylate/methacrylic acid=9/1 or 5/5 (molar ratio)) grains,and polystyrene grains. The grain diameter is preferably 0.8 to 10 μm,and a narrow grain diameter distribution is preferable. It is preferablethat 90% or more of all grains have grain diameters 0.9 to 1.1 times theaverage grain diameter. To increase the matting property, it ispreferable to simultaneously add fine grains with a grain size of 0.8 μmor smaller. Examples are polymethylmethacrylate grains (0.2 μm), poly(methylmethacrylate/methacrylic acid=9/1 (molar ratio), 0.3 μm) grains,and polystyrene grains (0.25 μm), and colloidal silica grains (0.03 μm).

Next, a film magazine (patrone) used in the present invention,preferably in the first embodiment is described below. The main materialof the magazine for use in the present invention, preferably in thefirst embodiment may be a metal or synthetic plastic.

Preferable plastic materials are polystyrenes, polyethylenes,polypropylenes, polyphenyl ethers, and the like. Further, the magazinethat can be used in the present invention, preferably in the firstembodiment may contain various antistatic agents, and preferably, forexample, carbon black, metal oxide particles; nonionic, anionic,cationic, and betaine-series surface-active agents, or polymers can beused. These antistatic magazines are described in JP-A-1-312537 andJP-A-1-312538. In particular, the resistance of the magazine at 25° C.and 25% RH is preferably 10¹²Ω or less. Generally, plastic magazines aremade of plastics with which carbon black or a pigment has been kneaded,to make the magazines shield (screen) light. The size of the magazinemay be size 135, which is currently used, and, to make cameras small, itis effective to change the diameter of the 25-mm cartridge of thecurrent size 135, to 22 mm or less. Preferably the volume of a case ofthe magazine is 30 cm³ or less, and more preferably 25 cm³ or less. Theweight of the plastic to be used for the magazine or the magazine caseis preferably 5 to 15 g.

Further, in the present invention, preferably in the first embodiment,the magazine may be one in which a spool is rotated to deliver a film.Also the structure may be such that the forward end of a film is housedin the magazine body, and by rotating a spool shaft in the deliveringdirection, the forward end of the film is delivered out from a port ofthe magazine. These magazines are disclosed in U.S. Pat. No. 4,834,306,and U.S. Pat. No. 5,226,613. A photographic film for use in the presentinvention, preferably in the first embodiment may be a so-called rawfilm, which is before being subjected to development, and may be aphotographic film after being processed. Further, a raw film and aphotographic film after development may be housed in the same newmagazine or in different magazines.

The color photographic light-sensitive material of the presentinvention, preferably of the first embodiment can be preferably usedalso as a negative film for advanced photo system (hereinafter referredto as AP system). Examples of the film include a film, manufactured bymaking the light-sensitive material film into AP system format andhousing it into a cartridge for exclusive use, such as NEXIA A, NEXIA F,and NEXIA H (trade names, ISO 200/100/400 in that order) manufactured byFuji Photo Film Co., Ltd. (hereinafter referred to as Fuji Film). Thesecartridge films for AP system are used after being loaded into camerasfor AP system, such as EPION series, e.g. EPION 300Z (trade name)manufactured by Fuji Film. The color photographic light-sensitivematerial of the present invention, preferably of the first embodiment isalso preferable for use in a film unit with a lens, which is representedby Fuji Color UTSURUNDESU Super Slim (trade name) manufactured by FujiFilm.

A film thus photographed is printed through the following steps in amini Lab system.

(1) Reception (an exposed cartridge film is received from a customer)

(2) Detaching step (the film is transferred from the cartridge to anintermediate cartridge for development steps)

(3) Film development

(4) Reattaching step (the developed negative film is returned to theoriginal cartridge)

(5) Printing (prints of three types C, H, and P and an index print arecontinuously automatically printed on color paper {preferably Fuji FilmSUPER FA8 (trade name)})

(6) Collation and shipment (the cartridge and the index print arecollated by an ID number and shipped together with the prints)

As these systems, Fuji Film MINILAB CHAMPION SUPER FA-298, FA-278,FA-258, FA-238 (trade names) and Fuji Film DIGITAL LAB SYSTEM FRONTIER(trade name) are preferable. Examples of a film processor for MINILABCHAMPION are FP922AL, FP562B, FP562B AL, FP362B, and FP362B AL (tradenames), and recommended processing chemicals are FUJI COLOR JUST-ITCN-16L and CN-16Q (trade names). Examples of a printer processor arePP3008AR, PP3008A, PP1828AR, PP1828A, PP1258AR, PP1258A, PP728AR, andPP728A (trade names), and recommended processing chemicals are FUJICOLOR JUST-IT CP-47L and CP-40FAII (trade names). In FRONTIER SYSTEM,Scanner & Image Processor SP-1000 and Laser Printer & Paper ProcessorLP-1000P or Laser Printer LP-1000W (trade names) are used. Both adetacher used in the detaching step and a reattacher used in thereattaching step are preferably Fuji Film DT200 or DT100 and AT200 orAT100 (trade names), respectively.

The AP system can also be enjoyed by PHOTO JOY SYSTEM whose maincomponent is Fuji Film Digital Image Workstation ALADDIN 1000 (tradename). For example, a developed APS cartridge film is directly loadedinto ALADDIN 1000, or image information of a negative film, positivefilm, or print is input to ALADDIN 1000 by 35-mm Film Scanner FE-550 orFlat Head Scanner PE-550 (trade names). Obtained digital data can beeasily processed and edited. This data can be printed out by DigitalColor Printer NC-550AL (trade name) using a photo-fixing heat-sensitivecolor printing system or PICTROGRAPHY 3000 (trade name) using a laserexposure thermal development transfer system, or by existing laboratoryequipment through a film recorder. ALADDIN 1000 can also output digitalinformation directly to a floppy disk (registered trademark) or zipdisk, or to CD-R via a CD writer.

In a home, a user can enjoy photographs on a TV set, simply by loading adeveloped AP system cartridge film into Fuji Film Photo Player AP-1(trade name). Image information can also be continuously input to apersonal computer with a high speed, by loading a developed AP systemcartridge film into Fuji Film Photo Scanner AS-1 (trade name). Fuji FilmPhoto Vision FV-10 or FV-5 (trade names) can be used to input a film,print, or three-dimensional object, to a personal computer. Furthermore,image information recorded in a floppy disk (registered trademark), zipdisk, CD-R, or hard disk can be variously processed on a computer byusing Fuji Film Application Software Photo Factory. Fuji Film DigitalColor Printer NC-2 or NC-2D (trade names) using a photo-fixingheat-sensitive color printing system is suited to outputting highquality prints from a personal computer. To keep developed AP systemcartridge films, FUJICOLOR POCKET ALUBUM AP-5 POP L, AP-1 POP L, AP-1POP KG, or CARTRIDGE FILE 16 (trade names) is preferable.

In the case of applying the present invention, preferably the firstembodiment, to a reflective (base)-type photographic material,preferable as the silver halide grains in the silver halide emulsionthat can be used are cubic or tetradecahedral crystal grainssubstantially having a {100} plane (the grain may have a round apex anda plane of a higher order); octahedral crystal grains; and tabulargrains having an aspect ratio of 2 or more, in which 50% or more of thetotal projected area thereof is taken up by a {100} plane or {111}plane. The aspect ratio is defined as the value obtained by dividing thediameter of a circle corresponding to the circle having the same area asa projected area of an individual grain by the thickness of the grain.In the present invention, preferably in the first embodiment, cubicgrains, or tabular grains having {100} planes as major faces, or tabulargrains having {111} planes as major faces are preferably used.

As a silver halide emulsion, any of silver chloride, silver bromide,silver iodobromide, or silver chloro(iodo)bromide emulsions may be used.It is preferable for a rapid processing to use a silver chloride, silverchlorobromide, silver chloroiodide, or silver chlorobromoiodideemulsions having a silver chloride content of 90 mol % or greater, morepreferably said silver chloride, silver chlorobromide, silverchloroiodide, or silver chlorobromoiodide emulsions having a silverchloride content of 95 mol % or greater, particularly preferably 98 mol% or greater. Preferred of these silver halide emulsions are thosehaving in the shell parts of silver halide grains a silver iodochloridephase of 0.01 to 0.50 mol %, more preferably 0.05 to 0.40 mol %, per molof the total silver, in view of high sensitivity and excellent highillumination intensity exposure suitability. Further, especiallypreferred of these silver halide emulsions are those containing silverhalide grains having on the surface thereof a silver bromide localizedphase of 0.2 to 5 mol %, more preferably 0.5 to 3 mol %, per mol of thetotal silver, since both high sensitivity and stabilization ofphotographic properties are attained.

In the present invention, for example, in the reflective (base)-typesilver halide color photographic material, preferred examples of silverhalide emulsions and other materials (additives or the like) for use,photographic constitutional layers (arrangement of the layers or thelike), and processing methods for processing the photographic materialsand additives for processing are disclosed in JP-A-62-215272,JP-A-2-33144 and European Patent No. 0355660 A2. Particularly, thosedisclosed in European Patent No. 0355660 A2 are preferably used.Further, it is also preferred to use silver halide color photographiclight-sensitive materials and processing methods thereof disclosed in,for example, JP-A-5-34889, JP-A-4-359249, JP-A-4-313753, JP-A-4-270344,JP-A-5-66527, JP-A-4-34548, JP-A-4-145433, JP-A-2-854, JP-A-1-158431,JP-A-2-90145, JP-A-3-194539, JP-A-2-93641 and European PatentPublication No. 0520457 A2.

Examples of the supports that can be used in the present inventioninclude a reflective support, a transparent support, or the like.

In particular, as the above-described reflective support and silverhalide emulsion, as well as the different kinds of metal ions to bedoped in the silver halide grains, the storage stabilizers orantifogging agents of the silver halide emulsion, the methods ofchemical sensitization (sensitizers), the methods of spectralsensitization (spectral sensitizing dyes), the cyan, magenta, and yellowcouplers and the emulsifying and dispersing methods thereof, the dyestability-improving agents (stain inhibitors and discolorationinhibitors), the dyes (coloring layers), the kinds of gelatin, the layerstructure of the light-sensitive material, and the film pH of thelight-sensitive material, those described in the patent publications asshown in the following table are preferably used in the presentinvention. TABLE 1 Element JP-A-7-104448 JP-A-7-77775 JP-A-7-301895Reflective-type bases Column 7, line 12 to Column 35, line 43 to Column5, line 40 to Column 12, line 19 Column 44, line 1 Column 9, line 26Silver halide Column 72, line 29 to Column 44, line 36 to Column 77,line 48 to emulsions Column 74, line 18 Column 46, line 29 Column 80,line 28 Different metal ion Column 74, lines 19 Column 46, line 30 toColumn 80, line 29 to species to 44 Column 47, line 5 Column 81, line 6Storage stabilizers or Column 75, lines 9 to Column 47, lines 20 Column18, line 11 to antifoggants 18 to 29 Column 31, line 37 (Especially,mercaptoheterocyclic compounds) Chemical sensitizing Column 74, line 45to Column 47, lines 7 to Column 81, lines 9 to methods (Chemical Column75, line 6 17 17 sensitizers) Spectrally sensitizing Column 75, line 19to Column 47, line 30 to Column 81, line 21 to methods (Spectral Column76, line 45 Column 49, line 6 Column 82, line 48 sensitizers) Cyancouplers Column 12, line 20 to Column 62, line 50 to Column 88, line 49to Column 39, line 49 Column 63, line 16 Column 89, line 16 Yellowcouplers Column 87, line 40 to Column 63, lines 17 Column 89, lines 17Column 88, line 3 to 30 to 30 Magenta couplers Column 88, lines 4 toColumn 63, line 3 to Column 31, line 34 to 18 Column 64, line 11 Column77, line 44 and column 88, lines 32 to 46 Emulsifying and Column 71,line 3 to Column 61, lines 36 Column 87, lines 35 dispersing methods ofColumn 72, line 11 to 49 to 48 couplers Dye-image- Column 39, line 50 toColumn 61, line 50 to Column 87, line 49 to preservability Column 70,line 9 Column 62, line 49 Column 88, line 48 improving agents(antistaining agents) Anti-fading agents Column 70, line 10 to Column71, line 2 Dyes (coloring agents) Column 77, line 42 to Column 7, line14 to Column 9, line 27 to Column 78, line 41 Column 19, line 42, Column18, line 10 and Column 50, line 3 to Column 51, line 14 Gelatins Column78, lines 42 Column 51, lines 15 Column 83, lines 13 to 48 to 20 to 19Layer construction of Column 39, lines 11 Column 44, lines 2 to Column31, line 38 to light-sensitive to 26 35 Column 32, line 33 materialsFilm pH of light- Column 72, lines 12 sensitive materials to 28 Scanningexposure Column 76, line 6 to Column 49, line 7 to Column 82, line 49 toColumn 77, line 41 Column 50, line 2 Column 83, line 12 Preservatives inColumn 88, line 19 to developing solution Column 89, line 22

The silver halide color photosensitive material, for example, of areflective (support)-type, of the present invention can preferably beused in combination with the exposure and development systems describedin the following known materials. Example of the development systeminclude the automatic print and development system described inJP-A-10-333253, the photosensitive material conveying apparatusdescribed in JP-A-2000-10206, a recording system including the imagereading apparatus described in JP-A-11-215312, exposure systems with thecolor image recording method described in JP-A-11-88619 andJP-A-10-202950, a digital photo print system including the remotediagnosis method described in JP-A-10-210206, and a photo print systemincluding the image recording apparatus described in JP-A-2000-310822.

The preferred scanning exposure methods which can be applied to thepresent invention are described in detail in the table shown above.

It is preferred to use a band stop filter, as described in U.S. Pat. No.4,880,726, when the photographic material of the present invention issubjected to exposure with a printer. Color mixing of light can beeliminated and color reproducibility can remarkably be improved by theabove means.

In the present invention, a yellow microdot pattern may be previouslyformed by pre-exposure before giving an image information, to therebyperform a copy restraint, as described in European Patent Nos. 0789270A1 and 0789480 A1.

With respect to the processing of the photographic material of thepresent invention, processing materials and processing methods, asdisclosed in JP-A-2-207250, from page 26, right under column, line 1 topage 34, right upper column, line 9, and JP-A-4-97355, from page 5, leftupper column, line 17 to page 18, right under column, line 20, can bepreferably applied. Further, as preservatives which are used in thedeveloping solution, compounds described in the patent publications asshown in the above table can be preferably used.

Typically, color-development processing when hue and white backgroundpreferable in the present invention are adjusted, is one, using CP48SChemical (trade name) as a processing agent, and Minilabo “PP350” (tradename) manufactured by Fuji Photo Film Co., Ltd., which processingincludes: imagewise exposing a sample of a photosensitive material tolight through a negative having an average density; and processing witha processing solution that has undergone continuous processing performeduntil the volume of a color-developer replenisher becomes twice thevolume of a color-developer tank.

As a chemical of the processing agent, CP45X, or CP47L, manufactured byFuji Photo Film Co., Ltd., or RA-100, RA-4, manufactured by EastmanKodak Co., (each trade name), or the like may be used.

The coupler represented by formula (CC-I) will be explained in detail.

In the formula (CC-I), G_(a) represents —C(R₁₃)= or —N═, G_(b)represents —C(R₂₃)=when G_(a) represents —N═, or G_(b) represents—N=when G_(a) represents —C(R₂₃)=. R₂, and R₂₂ each represent anelectron attractive group of which the Hammett's substituent constantσ_(p) value is 0.20 or more and 1.0 or less. It is preferable that thesum of each σ_(p) value of R₂₁ and R₂₂ is 0.65 or more. The coupler tobe used in the present invention, preferably in the second embodiment,has excellent ability as a cyan coupler by introducing such a strongelectron-attractive group. The sum of each σ_(p) value of R₂₁ and R₂₂ ismore preferably 0.70 or more, and the upper limit of the sum isgenerally about 1.8.

In the present invention-, preferably in the second embodiment, R₂₁ andR₂₂ each are an electron attractive group of which the Hammett'ssubstituent constant σ_(p) value is 0.20 or more and 1.0 or less.Preferably R₂₁ and R₂₂ are electron attractive group of which the σ_(p)value is 0.30 or more and 0.8 or less.

The Hammett rule is an empirical rule proposed by L. P. Hammett in 1935to discuss quantitatively the influence of substituents on the reactionor equilibrium of benzene derivatives, and its validity is approvedwidely nowadays. The substituent constant determined with the Hammettrule includes σ_(p) value and σ_(m) value, and these values can be foundin many general literatures. For example, such values are described indetail in e.g. “Lange's Handbook of Chemistry”, 12th edition, (1979),edited by J. A. Dean (McGraw-Hill), “Kagaku No Ryoiki” (Region ofChemistry), extra edition, No. 122, pp. 96-103, (1979) (Nankodo), and“Chemical Reviews”, Vol. 91, pp. 165-195, (1991). In the presentinvention, preferably in the second embodiment, R₂₁ and R₂₂ are definedin terms of the Hammett substituent constant σ_(p), but this does notmean that the substituent is limited to those having a value known inthe literatures, which can be found in the above literatures; it isneedless to say that even if the value is unknown in any literature,substituents which can have the value in the range if measured accordingto the Hammett rule are also included in the present invention.

Specific examples of the electron-attracting group R₂₁ and R₂₂ whereinthe σ_(p) value is 0.20 or more and 1.0 or less, include an acyl group,acyloxy group, carbamoyl group, aliphatic oxycarbonyl group, aryloxycarbonyl group, cyano group, nitro group, dialkyl phosphono group,diaryl phosphono group, diaryl phosphinyl group, alkyl sulfinyl group,aryl sulfinyl group, alkyl sulfonyl group, aryl sulfonyl group,sulfonyloxy group, acylthio group, sulfamoyl group, thiocyanate group,thiocarbonyl group, alkyl group substituted with at least two or morehalogen atoms, alkoxy group substituted with at least two or morehalogen atoms, aryloxy group substituted with at least two or morehalogen atoms, alkylamino group substituted with at least two or morehalogen atoms, alkylthio group substituted with at least two or morehalogen atoms, aryl group substituted with another electron-attractinggroup with a σ_(p) value of 0.20 or more, heterocyclic group, chlorineatom, bromine atom, azo group, and selenocyanate group. Among thesesubstituents, those which can further have a substituent, may have thesubstituent such as those emplified as R₂₃ will be explained later.

It is to be noted that the aliphatic oxycarbonyl group may be providedwith a straight-chain, branched or cyclic aliphatic moiety which may besaturated or may have an unsaturated bond. The aliphatic oxycarbonylgroup includes alkoxycarbonyl, cycloalkoxycarbonyl, alkenyloxycarbonyl,alkynyloxycarbonyl and cycloalkenyloxycarbonyl, and the like.

Examples of the σ_(p) value of typical electron attractive groupsserving as 0.2 or more and 1.0 or less are as follows: bromine atom(0.23), chlorine atom (0.23), cyano group (0.66), nitro group (0.78),trifluoromethyl group (0.54), tribromomethyl group (0.29),trichloromethyl group (0.33), carboxyl group (0.45), acetyl group(0.50), benzoyl group (0.43), acetyloxy group (0.31),trifluoromethanesulfonyl group (0.92), methanesulfonyl group (0.72),benzenesulfonyl group (0.70), methanesulfinyl group (0.49), carbamoylgroup (0.36), methoxycarbonyl group (0.45), ethoxycarbonyl group (0.45),phenoxycarbonyl group (0.44), pyrazolyl group (0.37), methanesulfonyloxygroup (0.36), dimethoxyphosphoryl group (0.60) and sulfamoyl group(0.57).

R₂₁ preferably represents a cyano group, an aliphatic oxycarbonyl group(which is a straight-chain or branched alkoxycarbonyl,aralkyloxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl,cycloalkoxycarbonyl or cycloalkenyloxycarbonyl group having 2 to 36carbon atoms, e.g., methoxycarbonyl, ethoxycarbonyl, dodecyloxycarbonyl,octadecyloxycarbonyl, 2-ethylhexyloxycarbonyl, sec-butyloxycarbonyl,oleyloxycarbonyl, benzyloxycarbonyl, propargyloxycarbonyl,cyclopentyloxycarbonyl, cyclohexyloxycarbonyl or2,6-di-t-butyl-4-methylcyclohexyloxycarbonyl), a dialkylphosphono group(which is a dialkylphosphono group having 2 to 36 carbon atoms, e.g.,diethylphosphono or dimethylphosphono), an alkyl- or aryl-sulfonyl group(which is an alkyl- or aryl-sulfonyl group having 1 to 36 carbon atoms,e.g., methanesulfonyl group, butanesulfonyl group, benzenesulfonyl groupor p-toluenesulfonyl group) or a fluorinated alkyl group (which is afluorinated alkyl group having 1 to 36 carbon atoms, e.g.,trifluoromethyl). R₂₁ is particularly preferably a cyano group,aliphatic oxycarbonyl group or fluorinated alkyl group, and mostpreferably a cyano group.

R₂₂ preferably represents an aliphatic oxycarbonyl group such as thoseexemplified as R₂₁, carbamoyl group (which is a carbamoyl group having 1to 36 carbon atoms, e.g., diphenylcarbamoyl or dioctylcarbamoyl),sulfamoyl group (which is a sulfamoyl group having 1 to 36 carbon atoms,e.g., dimethylsulfamoyl or dibutylsulfamoyl), dialkylphosphono groupsuch as those exemplified as R₂₁, or diarylphosphono group (which is adiarylphosphono group having 12 to 50-carbon atoms, e.g.,diphenylphosphono or di(p-toluoyl)phosphono). R₂₂ is particularlypreferably an aliphatic oxycarbonyl group represented by the followingformula.

In the formula, R₁′ and R₂′ respectively represent an aliphatic group,e.g., a straight-chain or branched alkyl, aralkyl, alkenyl, alkynyl,cycloalkyl or cycloalkenyl group having 1 to 36 carbon atoms,specifically, e.g., methyl, ethyl, propyl, isopropyl, t-butyl, t-amyl,t-octyl, tridecyl, cyclopentyl or cyclohexyl. R₃′, R₄′ and R₅′respectively represent a hydrogen atom or an aliphatic group. Examplesof the aliphatic group include those previously exemplified as R₁′ andR₂′. R₃′, R₄′ and R₅′ each are preferably a hydrogen atom.

W represents a nonmetallic atomic group required to form a five- toeight-membered ring, which may be substituted, may be a saturated ringand may have an unsaturated bond. Preferable examples of the nonmetallicatom include a nitrogen atom, oxygen atom, sulfur atom or carbon atom,and a carbon atom is a most preferable example.

Examples of the ring formed by W include, e.g., a cyclopentane ring,cyclohexane ring, cycloheptane ring, cyclooctane ring, cyclohexene ring,piperazine ring, oxane ring and thiane ring. These rings may besubstituted with a substituent such as those represented by R₂₃ as willbe explained later.

The ring formed by W is preferably a cyclohexane ring which may besubstituted, and particularly preferably a cyclohexane ring whose fourthposition is substituted with an alkyl group (which may be substitutedwith a substituent such as those represented by R₂₃ as will be explainedlater) having 1 to 36 carbon atoms.

R₂₃ represents a substituent.

Examples of the substituent represented by R₂₃ include alkyl groups(e.g., methyl, ethyl, isopropyl, t-butyl, t-amyl, adamantyl,1-methylcyclopropyl, t-octyl, cyclohexyl, 2-methanesulfonylethyl,3-(3-pentadecylphenoxy)propyl,3-{4-{2-[4-(4-hydroxyphenylsulfonyl)phenoxy]dodecanamido}phenyl}propyl,2-ethoxytridecyl, trifluoromethyl, cyclopentyl and3-(2,4-di-t-amylphenoxy)propyl), aralkyl groups (e.g., benzyl,4-methoxybenzyl and 2-methoxybenzyl), aryl groups (e.g., phenyl,4-t-butylphenyl, 2,4-di-t-amylphenyl and 4-tetradecanamidophenyl),alkoxy groups (e.g., methoxy, ethoxy, 2-methoxyethoxy, 2-dodecylethoxy,2-methanesulfonylethoxy and 2-phenoxyethoxy), aryloxy groups (e.g.,phenoxy, 2-methylphenoxy, 4-t-butylphenoxy, 3-nitrophenoxy,3-t-butyloxycarbamoylphenoxy and 3-methoxycarbamoylphenoxy), aminogroups (including anilino groups; e.g., methylamino, ethylamino,anilino, dimethylamino, diethylamino, t-butylamino, 2-methoxyanilino,3-acetylaminoanilino and cyclohexylamino), acylamino groups (e.g.,acetamide, benzamide, tetradecanamide,2-(2,4-di-t-amylphenoxy)butanamide,4-(3-t-butyl-4-hydroxyphenoxy)butanamide,2-{4-(4-hydroxyphenylsulfonyl)phenoxy}decanamide), ureido groups (e.g.,phenylureido, methylureido and N,N-dibutylureido), alkylthio groups(e.g., methylthio, octylthio, tetradecylthio, 2-phenoxyethylthio,3-phenoxypropylthio and 3-(4-t-butylphenoxy)propylthio), arylthio groups(e.g., phenylthio, 2-butoxy-5-t-octylphenylthio, 3-pentadecylphenylthio,2-carboxyphenylthio and 4-tetradecanamidophenylthio),alkoxycarbonylamino groups (e.g., methoxycarbonylamino andtetradecyloxycarbonylamino), carbamoyloxy groups (e.g.,N-methylcarbamoyloxy and N-phenylcarbamoyloxy) and heterocyclic thiogroups (e.g., 2-benzothiazolylthio, 2,4-di-phenoxy-1,3,5-triazole-6-thioand 2-pyridylthio).

R₂₃ is preferably a substituent selected from an aliphatic group, arylgroup, alkoxy group, aryloxy group, amino group, acylamino group,arylthio group, alkylthio group, ureido group, alkoxycarbonylaminogroup, carbamoyloxy group and heterocyclic thio group. These groups maybe substituted with a substituent (the substituents represented by R₂₃shown in the following).

R₂₃ is more preferably an aliphatic group (preferably an alkyl group oraralkyl group), aryl group, alkoxy group or acylamino group. Thesegroups may be substituted with a substituent exemplified as R₂₃.

Y represents a hydrogen atom or a group capable of being split-off upona coupling reaction with an oxidant of a developing agent.

Y is preferably a hydrogen atom, halogen atom, aryloxy group,heterocyclic acyloxy group, dialkylphosphonooxy group, arylcarbonyloxygroup, arylsulfonyloxy group, alkoxycarbonyloxy group or carbamoyloxygroup. Further, the split-off group (releasing group) or a compoundreleased from the split-off group preferably has the property of furtherreacting with an oxidant of a developing agent (preferably an oxidant ofan aromatic primary amine color-developing agent). Examples of thesplit-off group include non-color-forming couplers, hydroquinonederivatives, aminophenol derivatives and sulfonamidophenol derivatives.

As to the couplers represented by the formula (CC-I), the group of R₂₂or R₂₃ may contain a group to give a coupler represented by the formula(CC-I), to form a dimer or a polymer larger than a dimer; or the groupof R₂₂ or R₂₃ may contain a high molecular chain, to form a homopolymeror copolymer. Typical examples of the homopolymer or copolymercontaining a high molecular chain are homopolymers or copolymers ofaddition polymer ethylene-type unsaturated compounds having a group togive a coupler represented by the formula (CC-I). In this case, one ormore types of cyan color-forming repeating unit having a group to give acoupler represented by the formula (CC-I) may be contained in thepolymer. The coupler may be copolymers containing one or morenon-color-forming ethylene-type monomers which do not couple with anoxidant of a developing agent, for example, acrylates, methacrylates andmaleates as a copolymer component.

Hereinafter, specific examples of the couplers represented by formula(CC-I) are shown below, but the couplers for use in the presentinvention are not limited to these examples.

The coupler represented by the formula (CC-I) may be synthesized usingknown methods, for example, methods described in J.C.S., (1961), p. 518,J.C.S., (1962), p. 5149, Angew. Chem., Vol. 72, p. 956 (1960), andBerichte, Vol. 97, p. 3436 (1964), and methods described in thereferences cited therein or similar methods.

The couplers represented by any one of the formula (I), (II) or (CC-I)can be introduced into the light-sensitive material by using variousknown dispersing methods, among which an oil-in-water dispersing methodis preferable in which the coupler is dissolved in a high-boiling pointorganic solvent (which may be used together with a low-boiling pointsolvent, if necessary) and is then emulsified and dispersed in anaqueous gelatin solution, which is then added to the silver halideemulsion.

Examples of the high-boiling point solvent that can be used in thisoil-in-water dispersing method are described in U.S. Pat. No. 2,322,027and the like. Specific examples of the step and effect of a latexdispersing method, as one of polymer dispersing methods, and the latexfor impregnation, are described in, for example, U.S. Pat. No.4,199,363, West German Patent Application (OLS) Nos. 2,541,274 and2,541,230, JP-B-53-41091 and European Patent (Laid-Open) No. 029104.Also, particulars as to dispersion using an organic solvent-solublepolymer are described in the specification of PCT International PatentApplication (Laid-Open) No. WO88/00723.

Examples of the high-boiling point solvent which may be used in theaforementioned oil-in-water dispersing method, include phthalates (e.g.,dibutyl phthalate, dioctyl phthalate, dicyclohexyl phthalate,di-2-ethylhexyl phthalate, decyl phthalate,bis(2,4-di-tert-amylphenyl)isophthalate andbis(1,1-diethylpropyl)phthalate), phosphates or phosphonates (e.g.,diphenyl phosphate, triphenyl phosphate, tricresyl phosphate,2-ethylhexyldiphenyl phosphate, dioctylbutyl phosphate, tricyclohexylphosphate, tri-2-ethylhexyl phosphate, tridodecyl phosphate anddi-2-ethylhexylphenyl phosphate), citrates (e.g., tributyl citrate andtrihexyl citrate), benzoates (e.g., 2-ethylhexyl benzoate,2,4-dichlorobenzoate, dodecyl benzoate and2-ethylhexyl-p-hydroxybenzoate), amides (e.g., N,N-diethyldodecanamideand N,N-diethyllaurylamide), alcohols or phenols (e.g., isostearylalcohol and 2,4-di-tert-amylphenol), aliphatic esters (e.g.,dibutoxyethyl succinate, di-2-ethylhexyl succinate, 2-hexyldecyltetradecanate, tributyl citrate, diethyl azelate, isostearyl lactate andtrioctyl tosylate), aniline derivatives (e.g.,N,N-dibutyl-2-butoxy-5-tert-octylaniline), chlorinated paraffins(paraffins containing 10% to 80% of chlorine), trimesates (e.g.,tributyl trimesate), dodecylbenzene, diisopropylnaphthalene, phenols(e.g., 2,4-di-tert-amylphenol, 4-dodecyloxyphenol,4-dodecyloxycarbonylphenol and 4-(4-dodecyloxyphenylsulfonyl)phenol),carboxylates (e.g., 2-(2,4-di-tert-amylphenoxybutyric acid and2-ethoxyoctadecanic acid), and alkyl phosphoric acids (e.g.,di-(2-ethylhexyl)phosphoric acid and diphenylphosphoric acid). Besidesthe above high-boiling point solvents, compounds described in, forexample, JP-A-6-258803 are also preferably used as the high-boilingpoint solvent.

Among these solvents, phosphates are preferable and also alcohols orphenols are preferably used together the phosphates.

In the silver halide photographic light-sensitive material of thepresent invention, preferably of the second embodiment, the ratio bymass of the high-boiling point organic solvent to be used together withthe coupler represented by any of the aforementioned formula (I), (II)or (CC-I) to the coupler is preferably 0 to 2.0, more preferably 0 to1.0, and particularly preferably 0 to 0.5.

Also, an organic solvent (e.g., ethyl acetate, butyl acetate, ethylpropionate, methyl ethyl ketone, cyclohexanone, 2-ethoxyethyl acetateand dimethylformamide) having a boiling point of 30° C. or more andabout 160° C. or less, may be used together as an auxiliary solvent.

In the silver halide photographic light-sensitive material of thepresent invention, preferably of the second embodiment, the content ofthe coupler represented by any of the aforementioned formulae (1), (II)or (CC-I) in the light-sensitive material, is preferably 0.01 to 10g/m², and more preferably 0.1 to 2 g/m². The content of the coupler ispreferably 1×10⁻³ mol to 1 mol, and more preferably 2×10⁻³ mol to 3×10⁻¹mol, per mol of the silver halide contained in the same light-sensitiveemulsion layer.

Hereinafter, the silver halide color photographic light-sensitivematerial of the present invention (hereinafter, also referred to simplyas “a light-sensitive (or photosensitive) material”) is explained indetail.

In the present invention, preferably in the second and thirdembodiments, a silver halide color photosensitive material which has, ona support, at least one silver halide emulsion layer containing a yellowdye-forming coupler, at least one silver halide emulsion layercontaining a magenta dye-forming coupler, and at least one silver halideemulsion layer containing a cyan dye-forming coupler, is preferablyused.

In the present invention, preferably in the second and thirdembodiments, the silver halide emulsion layer containing a yellowdye-forming coupler functions as a yellow color-forming layer, thesilver halide emulsion layer containing a magenta dye-forming couplerfunctions as a magenta color-forming layer, and the silver halideemulsion layer containing a cyan dye-forming coupler functions as a cyancolor-forming layer. Preferably, the silver halide emulsions containedin the yellow color-forming layer, the magenta color-forming layer, andthe cyan color-forming layer may have photosensitivities to mutuallydifferent wavelength regions (for example, light in a blue region, lightin a green region and light in a red region).

In addition to the yellow color-forming layer, the magenta color-forminglayer, and the cyan color-forming layer, the photosensitive material ofthe present invention, preferably of the second and third embodiments,may have a hydrophilic colloid layer, an antihalation layer, anintermediate layer, and a coloring layer, as described below, ifnecessary.

The silver halide photographic light-sensitive material of the presentinvention, preferably of the second, third and fourth embodiments, canbe used in such applications as a color negative film, a color positivefilm, a color reversal film, a color reversal printing paper, a colorprinting paper, a color negative film for movies, a color positive filmfor movies, a display light-sensitive material, a color proof (digitalcolor proof in particular) light-sensitive material.

In the present invention, preferably in the second, third and fourthembodiments, preferred applications are a light-sensitive material to beused in direct appreciation, a color printing paper (color paper), adisplay light-sensitive material, a color proof, a color reversal film(color reversal), a color reversal printing paper, and a color positivefilm for movies. Among these applications, a color printing paper and acolor reversal film are preferable.

In case where the present invention, preferably the second, third andfourth embodiments, is applied to a color paper, the light-sensitivematerial and the like described in JP-A-11-7109, particularlydescriptions in paragraph numbers 0071 to 0087 in JP-A-11-7109 arepreferable, and therefore the above descriptions in JP-A-11-7109 areincorporated herein by reference.

In case where the present invention, preferably the second, third andfourth embodiments, is applied to a color negative film, thedescriptions in paragraph Nos. 0115 to 0217 of the specification ofJP-A-11-305396 can be preferably applied thereto, and therefore thedescriptions are incorporated herein by reference.

In case where the present invention, preferably the second, third andfourth embodiments, is applied to a color reversal film, thelight-sensitive material described in JP-A-2001-142181 is preferable,and the descriptions in paragraph Nos. 0164 to 0188 of the specificationof JP-A-2001-142181 and the descriptions in paragraph Nos. 0018 to 0021of the specification of JP-A-11-84601 can be preferably applied thereto,and therefore these descriptions are incorporated herein by reference.

The silver halide light-sensitive material that can be preferably usedin the present invention, preferably in the second and thirdembodiments, is explained below in detail.

Preferable as the silver halide grains in the silver halide emulsionthat can be used in the present invention, preferably in the second andthird embodiments, are cubic or tetradecahedral crystal grainssubstantially having a {100} plane (each grain may have a round apex anda plane of a higher order); octahedral crystal grains; and tabulargrains having an aspect ratio of 2 or more in which 50% or more of thetotal projected area thereof is taken up by a {100} plane or {111}plane. The aspect ratio is defined as the value obtained by dividing thediameter of a circle whose area is equal to the projected area of anindividual grain by the thickness of the grain. In the presentinvention, preferably in the second and third embodiments, cubic grains,or tabular grains having {100} planes as major faces, or tabular grainshaving {111} planes as major faces are preferably used.

As a silver halide emulsion which can be used in the present invention,preferably in the second and third embodiments, for example, silverchloride, silver bromide, silver iodobromide, or silverchloro(iodo)bromide emulsion may be used. It is preferable, for thepurpose of rapid processing, to use a silver chloride, silverchlorobromide, silver chloroiodide, or silver chlorobromoiodide emulsionhaving a silver chloride content of 90 mol % or greater, more preferablya silver chloride, silver chlorobromide, silver chloroiodide, or silverchlorobromoiodide emulsion having a silver chloride content of 98 mol %or greater. Preferred of these silver halide emulsions are those havingin the shell parts of silver halide grains a silver iodochloride phaseof 0.01 to 0.50 mol %, more preferably 0.05 to 0.40 mol %, per mol ofthe total silver, in view of high sensitivity and excellenthigh-illumination intensity exposure suitability. Further, especiallypreferred of these silver halide emulsions are those containing silverhalide grains having on the surface thereof a silver bromide localizedphase of 0.2 to 5 mol %, more preferably 0.5 to 3 mol %, per mol of thetotal silver, since both of high sensitivity and stabilization ofphotographic properties are attained.

To silver halide grains in the silver halide emulsion that can be usedin the present invention, preferably in the second and thirdembodiments, iodide ions are introduced to make the grain include silveriodide. In order to introduce iodide ions, an iodide salt solution maybe added singly, or it may be added in combination with both of a silversalt solution and a high chloride salt solution. In the latter case, theiodide salt solution and the high chloride salt solution may be addedseparately, or as a mixture solution of these salts of iodide and highchloride. The iodide salt is generally added in the form of a solublesalt, such as an alkali or alkali earth iodide salt. Alternatively,iodide ions may be introduced by cleaving the iodide ions from anorganic molecule, as described in U.S. Pat. No. 5,389,508. As anothersource of iodide ion, fine silver iodide grains may be used.

The addition of an iodide salt solution may be concentrated at one timeof grain formation process or may be performed over a certain period oftime. For obtaining an emulsion with high sensitivity and low fog, theposition of the introduction of an iodide ion to a high silver chlorideemulsion is restricted. The deeper in the emulsion grain the iodide ionis introduced, the smaller is the increment of sensitivity. Accordingly,the addition of an iodide salt solution is preferably started at 50% orouter side of the volume of a grain, more preferably 70% or outer side,and most preferably 80% or outer side. Moreover, the addition of aniodide salt solution is preferably finished at 98% or inner side of thevolume of a grain, more preferably 96% or inner side. When the additionof an iodide salt solution is finished at a little inner side of thegrain surface, an emulsion having higher sensitivity and lower fog canbe obtained.

The distribution of an iodide ion concentration in the depth directionof a grain can be measured according to an etching/TOF-SIMS (Time ofFlight-Secondary Ion Mass Spectrometry) method by means of, for example,a TRIFT II Model TOF-SIMS apparatus (trade name, manufactured by PhiEvans Co.). A TOF-SIMS method is specifically described in edited byNippon Hyomen Kagakukai, Hyomen Bunseki Gijutsu Sensho Niji Ton ShisuryoBunsekiho (Surface Analysis Technique Selection-Secondary Ion MassAnalytical Method), Maruzen Co., Ltd. (1999). When an emulsion grain isanalyzed by the etching/TOF-SIMS method, it can be analyzed that iodideions ooze toward the surface of the grain, even though the addition ofan iodide salt solution is finished at an inner side of the grain. It ispreferred that when the silver halide emulsion for use in the presentinvention, preferably in the second and third embodiments, containssilver iodide, the silver halide grains have the maximum concentrationof iodide ions at the surface of the grain, and the iodide ionconcentration decreases inwardly in the grain, for the analysis withetching/TOF-SIMS.

It is preferable that the silver halide emulsion in the light-sensitivematerial of the present invention, preferably of the second and thirdembodiments, has a localized silver bromide phase.

In the case where a silver halide emulsion for use in the presentinvention, preferably in the second and third embodiments, has alocalized silver bromide phase, it is preferable to prepare silverhalide grains by epitaxially growing, on the grain surface, thelocalized silver bromide phase having a silver bromide content of atleast 10 mol % or more. It is also preferable to have an outermost shellportion having a silver bromide content of 1 mol % or more in thevicinity of the surface layer.

The silver bromide content of the localized silver bromide phase ispreferably in the range of 1 to 80 mol % and most preferably in therange of 5 to 70 mol %. The localized silver bromide phase is made up ofpreferably 0.1 to 30 mol % of silver, more preferably 0.3 to 20 mol % ofsilver, based on the total moles of silver constituting the silverhalide grains in the present invention, preferably in the second andthird embodiments. It is preferable to incorporate a complex ion of aGroup VIII metal, such as an iridium ion, into the localized silverbromide phase. The amount of the compound (complex) to be added varieswidely depending on purposes, and the amount in the range of 10⁻⁹ to10⁻² mol, per mole of silver halide, is preferable.

In the present invention, preferably in the second and thirdembodiments, it is preferable to incorporate metal ions into theinterior and/or surface of silver halide grains, by the addition oftransition metal ions at a step in which the silver halide grains areformed and/or grown. As the metal ion that can be used, a transitionmetal ion is preferable. Among the transition metal ions, ions of iron,ruthenium, iridium, osmium, lead, cadmium or zinc are preferable. It isstill more preferable that these metal ions are used in the form of asix-coordination complex of octahedron-type having ligands. Whenemploying an inorganic compound as a ligand, a cyanide ion, halide ion,thiocyanato, hydroxide ion, peroxide ion, azide ion, nitrite ion, water(aquo), ammonio, nitrosyl ion, or thionitrosyl ion is preferably used.Such a ligand is preferably coordinated to any metal ion selected fromthe group consisting of the above-mentioned iron, ruthenium, iridium,osmium, lead, cadmium and zinc. Two or more kinds of these ligands arealso preferably used in one complex molecule.

In order to alleviate high-intensity illumination reciprocity failurefor the silver halide emulsion in the present invention, preferably inthe second and third embodiments, it is particularly preferable thatsilver halide grains of the emulsion has (is doped with) an iridium ionhaving at least one organic ligand.

In the case where an organic compound is used as the ligand, as a commonpractice with other transition metal, preferred examples of the organiccompound include a linear compound whose main chain has 5 or less carbonatoms and/or a 5-membered or 6-membered heterocyclic compound. Morepreferable examples of the organic compound are those having at least anitrogen, phosphorus, oxygen, or sulfur atom in a molecule as an atomwhich is capable of coordinating to a metal. Most preferred organiccompounds are furan, thiophene, oxazole, isooxazole, thiazole,isothiazole, imidazole, pyrazole, triazole, furazane, pyran, pyridine,pyridazine, pyrimidine and pyrazine. Further, organic compounds whichhave a substituent introduced into a basic skeleton of theabove-mentioned compounds are also preferred.

Among these compounds, a thiazole ligand, in particular5-methylthiazole, is used as a ligand particularly preferable to aniridium ion.

Preferable combinations of a metal ion and a ligand are those of ironand/or ruthenium ion and cyanide ion. Preferred of these compounds arethose in which the number of cyanide ions accounts for the majority ofthe coordination sites intrinsic to the iron or ruthenium that is thecentral metal. The remaining coordination sites are preferably occupiedby thiocyan, ammonia, water, nitrosyl ion, dimethylsulfoxide, pyridine,pyrazine, or 4,4′-bipyridine. Most preferably, each of 6 coordinationsites of the central metal is occupied by a cyanide ion, to form ahexacyano iron complex or a hexacyano ruthenium complex. These metalcomplexes having cyanide ion ligands are preferably added, during grainformation, in an amount of 1×10⁻⁸ mol to 1×10⁻² mol, most preferably1×10⁻⁶ mol to 5×10⁻⁴ mol, per mol of silver.

The use of the iridium ion is not limited to the combination with theabove organic ligand. Preferred examples of the ligand include afluoride ion, a chloride ion, a bromide ion, and an iodide ion. Amongthese ions, the use of a chloride ion or a bromide ion is preferable.Preferred specific examples of the iridium complex include: [IrCl₆]³⁻,[IrCl₆]²⁻, [IrCl₅(H₂O)]²⁻, [IrCl₅(H₂O)]⁻, [IrCl₄(H₂O)₂]⁻,[IrCl₄(H₂O)₂]⁰, [IrCl₃(H₂O)₃]⁰, [IrCl₃(H₂O)₃]⁺, [IrBr₆]³⁻, [IrBr₆]²⁻,[IrBr₅(H₂O)]²⁻, [IrBr₅(H₂O)]⁻, [IrBr₄(H₂O)₂]⁻, [IrBr₄(H₂O)₂]⁰,[IrBr₃(H₂O)₃]⁰, and [IrBr₃(H₂O)₃]⁺, besides those having any of theabove organic ligands.

The amount of the iridium complex to be added during the silver halidegrain formation is preferably 1×10⁻¹⁰ to 1×10⁻³ moles and mostpreferably 1×10⁻⁸ to 1×10⁻⁵ moles per mole of silver. In the case whereruthenium or osmium is used as the central metal, it is also preferableto use a nitrosyl ion, a thionitrosyl ion, or water molecule togetherwith a chloride ion as a ligand. More preferred is the formation of apentachloronitrosyl complex, a pentachlorothionitrosyl complex, apentachloroaquo complex. It is also preferable to form a hexachlorocomplex. The amount of the complex to be added during the silver halidegrain formation is preferably 1×10⁻¹⁰ to 1×10⁻⁶ moles and morepreferably 1×10⁻⁹ to 1×10⁻⁶ moles per mole of silver.

In the present invention, preferably in the second and thirdembodiments, the above-mentioned complexes are preferably added directlyto the reaction solution at the time of silver halide grain formation,or indirectly to the grain-forming reaction solution via addition to anaqueous halide solution for forming silver halide grains or othersolutions, so that they are doped to the inside of the silver halidegrains. Further, it is also preferable to combine these methods, toincorporate the complex into the inside of the silver halide grains.

In case where these complexes are doped to the inside of the silverhalide grains, they are preferably uniformly distributed in the insideof the grains. On the other hand, as disclosed in JP-A-4-208936,JP-A-2-125245 and JP-A-3-188437, they are also preferably distributedonly in the grain surface layer. Alternatively they are also preferablydistributed only in the inside of the grain while the grain surface iscovered with a layer free from the complex. Further, as disclosed inU.S. Pat. Nos. 5,252,451 and 5,256,530, it is also preferred that thesilver halide grains are subjected to physical ripening with fine grainshaving complexes incorporated therein to modify the grain surface phase.Further, these methods may be used in combination. Two or more kinds ofcomplexes may be incorporated in the inside of an individual silverhalide grain. The halogen composition of the position into which thecomplex is incorporated is not particularly limited, and it is alsopreferable to incorporate the complex into any of a silver chloridelayer, a silver chlorobromide layer, a silver bromide layer, a silveriodochloride layer, and a silver iodobromide layer.

The silver halide grains contained in the silver halide emulsion for usein the present invention, preferably in the second and thirdembodiments, have an average grain size (the grain size herein means thediameter of the circle equivalent to the projected area of the grain,and the number average is taken as the average grain size) of preferablyfrom 0.01 μm to 2 μm.

With respect to the distribution of sizes of these grains, so calledmonodisperse emulsion having a variation coefficient (the value obtainedby dividing the standard deviation of the grain size distribution by theaverage grain size) of 20% or less, more preferably 15% or less, andfurther preferably 10% or less, is preferred. For obtaining a widelatitude, it is also preferred to blend the above-described monodisperseemulsions in the same layer or to form a multilayer structure using themonodisperse emulsions.

Various compounds or precursors thereof can be contained in the silverhalide emulsion for use in the present invention, preferably in thesecond, third and fourth embodiments, to prevent fogging from occurringor to stabilize photographic performance, during manufacture, storage orphotographic processing of the photosensitive material. Specificexamples of compounds useful for the above purposes are disclosed inJP-A-62-215272, pages 39 to 72, and they can be preferably used. Inaddition, 5-arylamino-1,2,3,4-thiatriazole compounds (the aryl residualgroup has at least one electron-attractive group) disclosed in EuropeanPatent No. 0447647 can also be preferably used.

Further, in order to enhance storage stability of the silver halideemulsion for use in the present invention, it is also preferred in thepresent invention, preferably in the second, third and fourthembodiments, to use hydroxamic acid derivatives described inJP-A-11-109576; cyclic ketones having a double bond adjacent to acarbonyl group, both ends of said double bond being substituted with anamino group or a hydroxyl group, as described in JP-A-11-327094(particularly compounds represented by formula (S1); the description inparagraph Nos. 0036 to 0071 of JP-A-11-327094 is incorporated herein byreference); sulfo-substituted catechols and hydroquinones described inJP-A-11-143011 (for example, 4,5-dihydroxy-1,3-benzenedisulfonic acid,2,5-dihydroxy-1,4-benzenedisulfonic acid, 3,4-dihydroxybenzenesulfonicacid, 2,3-dihydroxybenzenesulfonic acid, 2,5-dihydroxybenzenesulfonicacid, 3,4,5-trihydroxybenzenesulfonic acid, and salts of these acids);hydroxylamines represented by formula (A) in U.S. Pat. No. 5,556,741(the descriptions of column 4, line 56 to column 11, line 22 in U.S.Pat. No. 5,556,741 can be preferably applied to the present invention,and incorporated herein by reference), and water-soluble reducing agentsrepresented by formula (I), (II), or (III) of JP-A-11-102045.

A spectral sensitizing dye can be incorporated, for the purpose ofimparting sensitivity in a desired light wavelength region, so-calledspectral sensitivity, to the silver halide emulsion in each layer of thephotosensitive material of the present invention, preferably of thesecond, third and fourth embodiments.

Spectral sensitizing dyes which can be used in the photosensitivematerial of the present invention, preferably of the second, third andfourth embodiments, for spectral sensitization of blue, green and redlight regions include, for example, those disclosed by F. M. Harmer, inHeterocyclic Compounds-Cyanine Dyes and Related Compounds, John Wiley &Sons, New York, London (1964). Specific examples of compounds andspectral sensitization processes that are preferably used in the presentinvention include those described in JP-A-62-215272, from page 22, rightupper column to page 38. In addition, the spectral sensitizing dyesdescribed in JP-A-3-123340 are particularly preferred as red-sensitivespectral sensitizing dyes for silver halide emulsion grains having ahigh silver chloride content, from the viewpoint of stability,adsorption strength, temperature dependency of exposure, and the like.

The amount of these spectral sensitizing dyes to be added can be variedin a wide range depending on the occasion, and it is preferably in therange of 0.5×10⁻⁶ mole to 1.0×10⁻² mole, more preferably in the range of1.0×10⁻⁶ mole to 5.0×10⁻³ mole, per mole of silver halide.

The silver halide emulsions for use in the present invention, preferablyin the second, third and fourth embodiments, are generally chemicallysensitized. Chemical sensitization can be performed by utilizing asulfur sensitization, represented by the addition of an unstable sulfurcompound, noble metal sensitization represented by gold sensitization,and reduction sensitization, each singly or in combination thereof.Compounds that are preferably used for chemical sensitization includethose described in JP-A-62-215272, from page 18, right lower column topage 22, right upper column of these, gold-sensitized silver halideemulsion is particularly preferred, since a fluctuation in photographicproperties which occurs when scanning exposure with laser beams or thelike is conducted, can be further reduced by gold sensitization.

In order to conduct gold sensitization to the silver halide emulsionthat can be used in the present invention, preferably in the second,third and fourth embodiments, various inorganic gold compounds, gold (I)complexes having an inorganic ligand, and gold (I) compounds having anorganic ligand may be used. Inorganic gold compounds, such aschloroauric acid or salts thereof; and gold (I) complexes having aninorganic ligand, such as dithiocyanato gold compounds (e.g., potassiumdithiocyanatoaurate (I)), and dithiosulfato gold compounds (e.g.,trisodium dithiosulfatoaurate (I)), are preferably used.

As the gold (I) compounds having an organic ligand (organic compound),the bis gold (I) mesoionic heterocycles described in JP-A-4-267249, forexample, gold (I) tetrafluoroboratebis(1,4,5-trimethyl-1,2,4-triazolium-3-thiolate), the organic mercaptogold (I) complexes described in JP-A-11-218870, for example, potassiumbis(1-[3-(2-sulfonatobenzamido)phenyl]-5-mercaptotetrazole potassiumsalt) aurate (I) pentahydrate, and the gold (I) compound with a nitrogencompound anion coordinated therewith, as described in JP-A-4-268550, forexample, gold (I) bis(1-methylhydantoinate) sodium salt tetrahydrate,may be used. As the gold (I) compound having the organic ligand, onethat has been synthesized and isolated in advance may be used.Alternatively, it can be added to the emulsion by mixing an organicligand with an Au compound (for example, (tetra)chloroauric acid or itssalt), to generate a gold (I) compound in the system without isolation.Further, the gold (I) compound having an organic ligand may be generatedin an emulsion, by adding an organic ligand and an Au compound (forexample, (tetra)chloroauric acid or its salt) to the emulsionseparately. Also, the gold (I) thiolate compound described in U.S. Pat.No. 3,503,749, the gold compounds described in JP-A-8-69074,JP-A-8-69075 and JP-A-9-269554, and the compounds described in U.S. Pat.No. 5,620,841, U.S. Pat. No. 5,912,112, U.S. Pat. No. 5,620,841, U.S.Pat. No. 5,939,245, and U.S. Pat. No. 5,912,111 may be used.

The amount of these compounds to be added can be varied in a wide rangedepending on the occasion, and it is generally in the range of 5×10⁻⁷mole to 5×10⁻³ mole, preferably in the range of 5×10⁻⁶ mole to 5×10⁻⁴mole, per mole of silver halide.

The silver halide emulsion for use in the present invention ispreferably subjected to gold sensitization using a colloidal goldsulfide. A method of producing the colloidal gold sulfide is describedin, for example, Research Disclosure, No. 37154, Solid State Ionics,Vol. 79, pp. 60 to 66 (1995), and Compt. Rend. Hebt. Seances Acad. Sci.Sect. B, Vol. 263, p. 1328 (1966). Colloidal gold sulfide having variousgrain sizes are applicable, and even those having a grain diameter of 50nm or less are also usable. The amount of colloidal gold sulfide to beadded can be varied in a wide range depending on the occasion, and it isgenerally in the range of 5×10⁻⁷ mol to 5×10⁻³ mol, preferably in therange of 5×10⁻⁶ mol to 5×10⁻⁴ mol, in terms of gold atom, per mol ofsilver halide.

In the present invention, gold sensitization may be used in combinationwith other sensitizing methods, for example, sulfur sensitization,selenium sensitization, tellurium sensitization, reductionsensitization, or noble metal sensitization using a noble metal compoundother than gold compounds.

The light-sensitive material according to the present invention,preferably the second, third and fourth embodiments, preferablycontains, in their hydrophilic colloid layers, dyes (particularlyoxonole dyes and cyanine dyes) that can be discolored by processing, asdescribed in European Patent No. 0337490 A2, pages 27 to 76, for thepurpose to prevent irradiation or halation or to enhance safelightsafety (immunity). Further, dyes described in European Patent No.0819977 are also preferably used in the present invention, preferably inthe second, third and fourth embodiments. Among these water-solubledyes, some deteriorate color separation or safelight safety when used inan increased amount. Preferable examples of the dye which can be usedand which does not deteriorate color separation include water-solubledyes described in JP-A-5-127324, JP-A-5-127325 and JP-A-5-216185.

In the present invention, preferably in the second, third and fourthembodiments, it is possible to use a colored layer which can bediscolored during processing, in place of the water-soluble dye, or incombination with the water-soluble dye. The colored layer that can bediscolored with processing to be used, may contact with alight-sensitive emulsion layer directly, or indirectly through aninterlayer containing an agent for preventing color-mixing duringprocessing, such as gelatin and hydroquinone. The colored layer ispreferably provided as a lower layer (closer to a support) with respectto the emulsion layer which develops the same primary color as the colorof the colored layer. It is possible to provide colored layersindependently, each corresponding to respective primary colors.Alternatively, only one layer selected from them may be provided. Inaddition, it is possible to provide a colored layer subjected tocoloring so as to match a plurality of primary-color regions. About theoptical reflection density of the colored layer, it is preferred that,at the wavelength which provides the highest optical density in a rangeof wavelengths used for exposure (a visible-light region from 400 nm to700 nm for an ordinary printer exposure, and the wavelength of the lightgenerated from the light source in the case of scanning exposure), theoptical density is within the range of 0.2 to 3.0, more preferably 0.5to 2.5, and particularly preferably 0.8 to 2.0.

The colored layer described above may be formed by a known method. Forexample, there are a method in which a dye in a state of a dispersion ofsolid fine particles is incorporated in a hydrophilic colloid layer, asdescribed in JP-A-2-282244, from page 3, upper right column to page 8,and JP-A-3-7931, from page 3, upper right column to page 11, left undercolumn; a method in which an anionic dye is mordanted in a cationicpolymer, a method in which a dye is adsorbed onto fine grains of silverhalide or the like and fixed in the layer, and a method in which acolloidal silver is used as described in JP-A-1-239544. As to a methodof dispersing fine-powder of a dye in solid state, for example,JP-A-2-308244, pages 4 to 13 describes a method in which fine particlesof dye which is at least substantially water-insoluble at the pH of 6 orless, but at least substantially water-soluble at the pH of 8 or more,are incorporated. The method of mordanting anionic dyes in a cationicpolymer is described, for example, in JP-A-2-84637, pages 18 to 26. U.S.Pat. Nos. 2,688,601 and 3,459,563 disclose a method of preparing acolloidal silver for use as a light absorber. Among these methods,preferred are the methods of incorporating fine particles of dye and ofusing a colloidal silver.

In the case where the present invention, preferably the second, thirdand fourth embodiments, is applied to a color printing paper, the lightsensitive material preferably has at least one yellow color-formingsilver halide emulsion layer, at least one magenta color-forming silverhalide emulsion layer, and at least one cyan color-forming silver halideemulsion layer, on a support. Generally, these silver halide emulsionlayers are in the order, from the support, of the yellow color-formingsilver halide emulsion layer, the magenta color-forming silver halideemulsion layer and the cyan color-forming silver halide emulsion layer.

However, another layer arrangement which is different from the above,may be adopted.

In the light-sensitive material of the present invention, preferably ofthe second, third and fourth embodiments, a yellow coupler-containingsilver halide emulsion layer may be provided at any position on asupport. However, in the case where silver halide tabular grains arecontained in the yellow coupler-containing layer, it is preferable thatthe yellow coupler-containing layer may be positioned more apart fromthe support than at least one of a magenta coupler-containing silverhalide emulsion layer and a cyan coupler-containing silver halideemulsion layer. Further, it is preferable that the yellowcoupler-containing silver halide emulsion layer be positioned most apartfrom the support than other silver halide emulsion layers, from theviewpoint of color-development acceleration, desilvering acceleration,and reducing residual color due to a sensitizing dye. Further, it ispreferable that the cyan coupler-containing silver halide emulsion layerbe provided in the middle of other silver halide emulsion layers, fromthe viewpoint of reducing blix fading. On the other hand, it ispreferable that the cyan coupler-containing silver halide emulsion layerbe the lowest layer, from the viewpoint of reducing light fading.Further, each of the yellow-color-forming layer, themagenta-color-forming layer and the cyan-color-forming layer may becomposed of two or three layers. It is also preferable that acolor-forming layer be formed by providing a silver halide emulsion-freelayer containing a coupler in adjacent to a silver halide emulsionlayer, as described in, for example, JP-A-4-75055, JP-A-9-114035,JP-A-10-246940, and U.S. Pat. No. 5,576,159.

In the present invention, preferably in the second, third, and fourthembodiments, for example, as a photographic support (base), atransmissive type support and a reflective type support may be used. Asthe transmissive type support, it is preferred to use a transparentfilm, such as a cellulose nitrate film, a transparent film ofpolyethylene terephthalate, a cellulose triacetate film, or a polyesterof 2,6-naphthalenedicarboxylic acid (NDCA) and ethylene glycol (EG), ora polyester of NDCA, terephthalic acid and EG, provided thereon with aninformation-recording layer such as a magnetic layer. In the presentinvention, preferably in the second, third and fourth embodiments, it ispreferable to use a reflective support (reflection-type support). As thereflective type support, it is especially preferable to use a reflectivesupport having a substrate laminated thereon with a plurality ofpolyethylene layers or polyester layers (water-proof resin layers orlaminate layers), at least one of which contains a white pigment such astitanium oxide.

As cyan, magenta and yellow couplers which can be used in the presentinvention, preferably in the second, third and fourth embodiments(including the case when these couplers are used in combination with thespecific coupler as defined in the present invention), in addition tothe above mentioned ones, those disclosed in JP-A-62-215272, page 91,right upper column, line 4 to page 121, left upper column, line 6,JP-A-2-33144, page 3, right upper column, line 14 to page 18, left uppercolumn, bottom line, and page 30, right upper column, line 6 to page 35,right under column, line 11, European Patent No. 0355,660 (A2), page 4,lines 15 to 27, page 5, line 30 to page 28, bottom line, page 45, lines29 to 31, page 47, line 23 to page 63, line 50, are also preferablyused.

Further, it is preferred in the present invention, preferably in thesecond, third and fourth embodiments, to add compounds represented byformula (II) or (III) in WO 98/33760 and compounds represented byformula (D) described in JP-A-10-221825.

The cyan dye-forming coupler (hereinafter also referred to as “cyancoupler”) which can be used in the present invention, preferably in thesecond embodiment, may be used singly or in combination with anothercyan coupler. Examples of the another cyan dye-forming coupler that maybe used in combination, include phenol-series or naphthol-series cyancouplers. For example, cyan couplers represented by formula (ADF)described in JP-A-10-333297 are preferred. As cyan couplers other thanthe foregoing cyan couplers, there are pyrroloazole-type cyan couplersdescribed in European Patent Nos. 0 488 248 and 0 491 197 (A1),2,5-diacylamino phenol couplers described in U.S. Pat. No. 5,888,716,pyrazoloazole-type cyan couplers having an electron-withdrawing group ora group bonding via hydrogen bond at the 6-position, as described inU.S. Pat. Nos. 4,873,183 and 4,916,051, and particularlypyrazoloazole-type cyan couplers having a carbamoyl group at the6-position, as described in JP-A-8-171185, JP-A-8-311360 andJP-A-8-339060.

In addition, the cyan dye-forming coupler can also be adiphenyllmidazole-series cyan coupler described in JP-A-2-33144; as wellas a 3-hydroxypyridine-series cyan coupler (particularly a 2-equivalentcoupler formed by allowing a 4-equivalent coupler of a coupler (42), tohave a chlorine splitting-off group, and couplers (6) and (9),enumerated as specific examples are particularly preferable) describedin EP 0333185 A2; a cyclic active methylene-series cyan coupler(particularly couplers 3, 8, and 34 enumerated as specific examples areparticularly preferable) described in JP-A-64-32260; a pyrrolopyrozolecyan coupler described in European Patent No. 0456226 A1; and apyrroloimidazole cyan coupler described in European Patent No. 0484909.

As the magenta dye-forming coupler (which may be referred to simply as a“magenta coupler” herein) that can be used in the present invention,preferably in the second, third and fourth embodiments, use can be madeof 5-pyrazolone-series magenta couplers and pyrazoloazole-series magentacouplers such as those described in the above-mentioned patentpublications in the above tables. Among these, preferred arepyrazolotriazole couplers in which a secondary or tertiary alkyl groupis directly bonded to the 2-, 3- or 6-position of the pyrazolotriazolering, such as those described in JP-A-61-65245; pyrazoloazole couplershaving a sulfonamido group in its molecule, such as those described inJP-A-61-65246; pyrazoloazole couplers having an alkoxyphenylsulfonamidoballasting group, such as those described in JP-A-61-147254; andpyrazoloazole couplers having an alkoxy or aryloxy group at the6-position, such as those described in European Patent Nos. 0226849 A2and 0294785 A, in view of the hue and stability of image to be formedtherefrom and color-forming property of the couplers. Particularly asthe magenta coupler, pyrazoloazole couplers represented by formula(CC-I) described in JP-A-8-122984 are preferred. The descriptions ofparagraph Nos. 0009 to 0026 of the patent publication JP-A-8-122984 areentirely applied to the present invention and therefore are incorporatedby reference, in the specification as a part thereof. In addition,pyrazoloazole couplers having a steric hindrance group at both the 3-and 6-positions, as described in European Patent Nos. 854384 and 884640,JP-A-2000-147725, and JP-A-2001-356455, can also be preferably used.

Further, the yellow dye-forming coupler (which may be referred to simplyas a “yellow coupler” herein), that can be used in the presentinvention, preferably in the second and third embodiments, may be usedsingly or in combination with another yellow dye-forming coupler.Examples of the another yellow dye-forming coupler that can bepreferably used, include acylacetamide-type yellow couplers in which theacyl group has a 3-membered to 5-membered cyclic structure, such asthose described in European Patent No. 0447969 A1; malondianilide-typeyellow couplers having a cyclic structure, as described in EuropeanPatent No. 0482552 A1; pyrrol-2 or 3-yl- or indol-2 or 3-yl-carbonylacetic acid anilide-series couplers, as described in European Patent(laid open) Nos. 953870 A1, 953871 A1, 953872 A1, 953873 A1, 953874 A1and 953875 A1; acylacetamide-type yellow couplers having a dioxanestructure, such as those described in U.S. Pat. No. 5,118,599; inaddition to the compounds described in the above-mentioned tables. Amongthe above, acylacetamide-type yellow couplers in which the acyl group isan 1-alkylcyclopropane-1-carbonyl group, and malondianilide-type yellowcouplers in which one anilide constitutes an indoline ring areespecially preferably used. These couplers may be used singly or ascombined.

In the fourth embodiment of the present invention, as the yellowdye-forming coupler, the above-mentioned various compounds and thecompound represented by formula (1) may be used singly or incombination. Among these compounds, the compound represented by formula(I) is preferred.

It is preferred that couplers for use in the present invention,preferably in the second, third and fourth embodiments, are pregnatedinto a loadable latex polymer (as described, for example, in U.S. Pat.No. 4,203,716) in the presence (or absence) of the high-boiling-pointorganic solvent described in the foregoing table, or they are dissolvedin the presence (or absence) of the foregoing high-boiling-point organicsolvent with a polymer insoluble in water but soluble in an organicsolvent, and then emulsified and dispersed into an aqueous hydrophiliccolloid solution. Examples of the water-insoluble but organicsolvent-soluble polymer which can be preferably used, include thehomo-polymers and co-polymers as disclosed in U.S. Pat. No. 4,857,449,from column 7 to column 15 and WO 88/00723, from page 12 to page 30. Theuse of methacrylate-series or acrylamide-series polymers, especiallyacrylamide-series polymers, are more preferable, in view of color-imagestabilization and the like.

In the present invention, preferably in the second, third and fourthembodiments, known color mixing-inhibitors may be used. Among thesecompounds, those described in the following patent publications arepreferred.

For example, high molecular weight redox compounds described inJP-A-5-333501; phenidone- or hydrazine-series compounds as described in,for example, WO 98/33760 and U.S. Pat. No. 4,923,787; and white couplersas described in, for example, JP-A-5-249637, JP-A-10-282615 and GermanPatent No. 19629142 A1, may be used. Particularly, in order toaccelerate developing speed by increasing the pH of a developingsolution, redox compounds described in, for example, German Patent No.19,618,786 A1, European Patent Nos. 0,839,623 A1 and 0,842,975 A1,German Patent No. 19,806,846 A1 and French Patent No. 2,760,460 A1, arealso preferably used.

In the present invention, preferably in the second, third and fourthembodiments, as an ultraviolet ray absorbent, it is preferred to usecompounds having a high molar extinction coefficient and a triazineskeleton. For example, those described in the following patentpublications can be used. These compounds are preferably added to thelight-sensitive layer or/and the light-nonsensitive layer. For example,use can be made of the compounds described in JP-A-46-3335,JP-A-55-152776, JP-A-5-197074, JP-A-5-232630, JP-A-5-307232,JP-A-6-211813, JP-A-8-53427, JP-A-8-234364, JP-A-8-239368, JP-A-9-31067,JP-A-10-115898, JP-A-10-147577, JP-A-10-182621, German Patent No.19,739,797A, European Patent No. 0,711,804 A, JP-T-8-501291 (“JP-T”means searched and published International patent application), and thelike.

As the binder or protective colloid which can be used in thelight-sensitive material of the present invention, preferably of thesecond, third and fourth embodiments, gelatin is used advantageously,but another hydrophilic colloid can be used singly or in combinationwith gelatin. It is preferable for the gelatin that the content of heavymetals, such as Fe, Cu, Zn and Mn, contained as impurities, be reducedto 5 ppm or below, more preferably 3 ppm or below. Further, the amountof calcium contained in the light-sensitive material is preferably 20mg/m² or less, more preferably 10 mg/m² or less, and most preferably 5mg/m² or less.

In the present invention, preferably in the second, third and fourthembodiments, it is preferred to add an antibacterial (fungi-preventing)agent and antimold agent, as described in JP-A-63-271247, in order todestroy various kinds of molds and bacteria which propagate in ahydrophilic colloid layer and deteriorate the image. Further, the pH ofthe film of the light-sensitive material is preferably in the range of4.0 to 7.0, more preferably in the range of 4.0 to 6.5.

In the present invention, preferably in the second and thirdembodiments, a surface-active agent may be added to the light-sensitivematerial, in view of improvement in stability for coating thelight-sensitive material, prevention of static electricity from beingoccurred, and adjustment of the charge amount. As the surface-activeagent, there are anionic, cationic, betaine and nonionic surfactants.Examples thereof include those described in JP-A-5-333492. As thesurface-active agent for use in the present invention, preferably in thesecond and third embodiments, a fluorine-containing surface-active agentis particularly preferred. The fluorine-containing surface-active agentmay be used singly or in combination with known another surface-activeagent. The fluorine-containing surfactant is preferably used incombination with known another surface-active agent. The amount of thesurface-active agent to be added to the light-sensitive material is notparticularly limited, but it is generally in the range of 1×10⁻⁵ to 1g/m², preferably in the range of 1×10⁻⁴ to 1×10⁻¹ g/m², and morepreferably in the range of 1×10⁻³ to 1×10⁻² g/m².

The photosensitive material of the present invention, preferably of thesecond, third and fourth embodiments, can form an image, via an exposurestep in which the photosensitive material is irradiated with lightaccording to image information, and a development step in which thephotosensitive material irradiated with light is developed.

The light-sensitive material of the present invention, preferably of thesecond, third and fourth embodiments, can preferably be used, in ascanning exposure system using a cathode ray tube (CRT), in addition tothe printing system using a usual negative printer. The cathode ray tubeexposure apparatus is simpler and more compact, and therefore lessexpensive than an apparatus using a laser. Further, optical axis andcolor (hue) can easily be adjusted. In a cathode ray tube which is usedfor image-wise exposure, various light-emitting materials which emit alight in the spectral region, are used as occasion demands. For example,any one of red-light-emitting materials, green-light-emitting materials,blue-light-emitting materials, or a mixture of two or more of theselight-emitting materials may be used. The spectral regions are notlimited to the above red, green and blue, and fluorophoroes which canemit a light in a region of yellow, orange, purple or infrared can alsobe used. Particularly, a cathode ray tube which emits a white light bymeans of a mixture of these light-emitting materials, is often used.

In the case where the light-sensitive material has a plurality oflight-sensitive layers each having different spectral sensitivitydistribution from each other and also the cathode ray tube has afluorescent substance which emits light in a plurality of spectralregions, exposure to a plurality of colors may be carried out at thesame time. Namely, a plurality of color image signals may be input intoa cathode ray tube, to allow light to be emitted from the surface of thetube. Alternatively, a method in which an image signal of each of colorsis successively input and light of each of colors is emitted in order,and then exposure is carried out through a film capable of cutting acolor other than the emitted color, i.e., a surface successive exposure,may be used. Generally, among these methods, the surface successiveexposure is preferred from the viewpoint of high quality enhancement,because a cathode ray tube having a high resolving power can be used.

The light-sensitive material of the present invention, preferably of thesecond, third and fourth embodiments can preferably be used in thedigital scanning exposure system using monochromatic high density light,such as a gas laser, a light-emitting diode, a semiconductor laser, asecond harmonic generation light source (SHG) comprising a combinationof nonlinear optical crystal with a semiconductor laser or a solid statelaser using a semiconductor laser as an excitation light source. It ispreferred to use a semiconductor laser, or a second harmonic generationlight source (SHG) comprising a combination of nonlinear optical crystalwith a solid state laser or a semiconductor laser, to make a system morecompact and inexpensive. In particular, to design a compact andinexpensive apparatus having a longer duration of life and highstability, use of a semiconductor laser is preferable; and it ispreferred that at least one of exposure light sources would be asemiconductor laser.

When such a scanning exposure light source is used, the maximum spectralsensitivity wavelength of the light-sensitive material of the presentinvention, preferably of the second, third and fourth embodiments, canbe arbitrarily set up in accordance with the wavelength of a scanningexposure light source to be used. Since oscillation wavelength of alaser can be made half, using a SHG light source obtainable by acombination of a nonlinear optical crystal with a semiconductor laser ora solid state laser using a semiconductor as an excitation light source,blue light and green light can be obtained. Accordingly, it is possibleto have the spectral sensitivity maximum of a photographic material innormal three wavelength regions of blue, green and red. The exposuretime in such a scanning exposure is defined as the time necessary toexpose the size of the picture element (pixel) with the density of thepicture element being 400 dpi, and preferred exposure time is 10⁻³ secor less, more preferably 10⁻⁴ sec or less, and further preferably 10⁻⁶sec or less.

Moreover, the developing agent that can be used in the presentinvention, preferably in the fourth embodiment, is preferably ap-phenylenediamine-series aromatic primary amine developing agent.Representative examples of the developing agent include4-amino-3-methyl-N-ethyl-N—(β-methanesulfonamidoethyl)aniline,4-amino-3-methyl-N-ethyl-N-(β-hydroxyethyl)aniline, and4-amino-3-methyl-N,N-diethylaniline. Most preferred in the presentinvention, preferably in the fourth embodiment is4-amino-3-methyl-N-ethyl-N-(β-methanesulfonamidoethyl)aniline.

The present invention, preferably the second, third and fourthembodiments, can be preferably applied to a light-sensitive materialhaving rapid processing suitability. In the case of conducting rapidprocessing, the color-developing time is preferably 60 sec or less, morepreferably from 50 sec to 6 sec, and further preferably from 30 sec to 6sec. Likewise, the blix time is preferably 60 sec or less, morepreferably from 50 sec to 6 sec, and further preferably from 30 sec to 6sec. Further, the washing or stabilizing time is preferably 150 sec orless, and more preferably from 130 sec to 6 sec.

Herein, the term “color-developing time” as used herein means a periodof time required from the beginning of dipping a light-sensitivematerial into a color developing solution until the light-sensitivematerial is dipped into a blix solution in the subsequent processingstep. In the case where a processing is carried out using, for example,an autoprocessor, the color developing time is the sum total of a timein which a light-sensitive material has been dipped in acolor-developing solution (so-called “time in the solution”) and a timein which the light-sensitive material has left the color-developingsolution and been conveyed in air toward a bleach-fixing bath in thestep subsequent to color development (so-called “time in the air”).Likewise, the term “blix time” as used herein means a period of timerequired from the beginning of dipping a light-sensitive material into ablix solution until the light-sensitive material is dipped into awashing bath or a stabilizing bath in the subsequent processing step.Further, the term “washing or stabilizing time” as used herein means aperiod of time required from the beginning of dipping a light-sensitivematerial into a washing solution or a stabilizing solution until the endof the dipping toward a drying step (so-called “time in the solution”).

Examples of a development method applicable to the light-sensitivematerial of the present invention, preferably of the second, third andfourth embodiments, after exposure, include a conventional wet system,such as a development method using a developing solution containing analkali agent and a developing agent, and a development method wherein adeveloping agent is incorporated in the light-sensitive material and anactivator solution, e.g., a developing agent-free alkaline solution isemployed for the development, as well as a heat development system usingno processing solution. In particular, the activator method is preferredover the other methods, because the processing solutions contain nodeveloping agent, thereby it enables easy management and handling of theprocessing solutions and reduction in waste disposal load to make forenvironmental preservation.

The preferable developing agents or their precursors incorporated in thelight-sensitive materials in the case of adopting the activator methodinclude the hydrazine-type compounds described in, for example,JP-A-8-234388, JP-A-9-152686, JP-A-9-152693, JP-A-9-211814 andJP-A-9-160193.

Further, the processing method in which the photographic materialreduced in the amount of silver to be applied undergoes the imageamplification processing using hydrogen peroxide (intensificationprocessing), can be employed preferably. In particular, it is preferableto apply this processing method to the activator method. Specifically,the image-forming methods utilizing an activator solution containinghydrogen peroxide, as disclosed in JP-A-8-297354 and JP-A-9-152695 canbe preferably used. Although the processing with an activator solutionis generally followed by a desilvering step in the activator method, thedesilvering step can be omitted in the case of applying the imageamplification processing method to photographic materials having areduced silver amount. In such a case, washing or stabilizationprocessing can follow the processing with an activator solution toresult in simplification of the processing process. On the other hand,when the system of reading the image information from photographicmaterials by means of a scanner or the like is employed, the processingform requiring no desilvering step can be applied, even if thephotographic materials are those having a high silver amount, such asphotographic materials for shooting.

As the processing materials and processing methods of the activatorsolution, desilvering solution (bleach/fixing solution), washingsolution and stabilizing solution, which can be used in the presentinvention, preferably in the second, third and fourth embodiments, knownones can be used. Preferably, those described in Research Disclosure,Item 36544, pp. 536-541 (September 1994), and JP-A-8-234388 can be usedin the present invention, preferably in the second, third and fourthembodiments.

In the silver halide photographic light-sensitive material of thepresent invention, preferably of the third and fourth embodiments, thecontent of the coupler represented by the formula (I) or (II) preferablyused in the light-sensitive material is preferably 0.01 g to 10 g perm², more preferably 0.1 g to 2 g per m², and it is preferably 1×10⁻³ molto 1 mol, more preferably 2×10⁻³ mol to 3×10⁻¹ mol, per mol of thesilver halide in the same light-sensitive emulsion layer.

Next, the compound (a high-boiling-point organic solvent), which can beused in the present invention, preferably in the third embodiment, andwhich is represented by any one of the formula [S-I] to [S-VI], will beexplained in detail.

First, the high-boiling-point organic solvent, which is represented bythe formula [S-I], will be explained.

In the formula [S-I], R_(s1), R_(s2), and R_(s3) each independentlyrepresent an alkyl group, a cycloalkyl group, an alkenyl group, or anaryl group, with the proviso that the total of the carbon atoms of thegroups represented by R_(s1), R_(s2), and R_(s3) is 12 to 60.

The alkyl group is preferably a straight-chain or branched alkyl grouphaving 1 to 32 carbon atoms. These alkyl groups include those having asubstituent(s). Examples of the alkyl group include a straight-chain orbranched butyl group, hexyl group, octyl group, dodecyl group, octadecylgroup, and other groups. Among the alkyl groups, particularly preferredare those having 4 to 18 carbon atoms, and further preferred are thosehaving 6 to 12 carbon atoms.

Examples of the cycloalkyl group include a cyclopentyl group, acyclohexyl group, a cycloheptyl group, and other groups. Thesecycloalkyl groups include those having a substituent(s). Among thecycloalkyl groups, a cyclohexyl group is particularly preferable.

Examples of the alkenyl group include a butenyl group, a pentenyl group,a hexenyl group, a heptenyl group, an octenyl group, a decenyl group, adodecenyl group, an octadecenyl group and other groups. These alkenylgroups include those having a substituent(s).

Examples of the aryl group include a phenyl group, a naphthyl group, andother groups. These groups include those having a substituent(s).Specific examples of the aryl group include phenyl, p-cresyl, m-cresyl,o-cresyl, p-chlorophenyl, p-t-butyl-phenyl, and other groups.

Specific examples of the high-boiling-point organic solvent representedby the formula [S-I] will be shown below, but the present inventionshould not be considered to be limited thereto. No. Rs₁ Rs₂ Rs₃ S-I-1—C₆H₁₃ —C₆H₁₃ —C₆H₁₃ S-I-2 —C₈H₁₇ —C₈H₁₇ —C₈H₁₇ S-I-3 —C₁₂H₂₅ —C₁₂H₂₅—C₁₂H₂₅ S-I-4

S-I-5

S-I-6

S-I-7

S-I-8 —C₄H₉ —C₈H₁₇ —C₈H₁₇ S-I-9

S-I-10

S-I-11

S-I-12

—C₈H₁₇ —C₈H₁₇ S-I-13

—C₆H₁₃ —C₆H₁₃ S-I-14

S-I-15 —C₈H₁₇ —C₈H₁₇ —CH₂CH₂OCH₂CH₃ S-I-16

S-I-17 —CH₂CH₂C(CH₃)₃ —CH₂CH₂C(CH₃)₃ —CH₂CH₂C(CH₃)₃ S-I-18

S-I-19

S-I-20

S-I-21

S-I-22

The high boiling point organic solvents represented by the formula [S-I]include phosphoric ester-based compounds described, for example, inJP-B-48-32727, JP-A-53-13923, JP-A-54-119235, JP-A-54-119921,JP-A-59-119922, JP-A-55-25057, JP-A-55-36869, JP-A-56-81836, and thelike. The high boiling point organic solvents can be synthesizedaccording to the methods described in these official gazettes.

Next, the high boiling point organic solvent, which is represented bythe formula [S-II], will be explained in detail.

In the formula [S-II], an alkyl group or a cycloalkyl group representedby R_(s4) and R_(s5) is preferably an alkyl group or a cycloalkyl grouphaving 1 to 20 carbon atoms. Examples thereof include a methyl group, anethyl group, a butyl group, a dodecyl group, an eicosyl group, ani-propyl group, a t-butyl group, a t-pentyl group, an i-butyl group, a1,1-dimethylbutyl group, a 1,1,3,3-tetramethylbutyl group, a2-ethylhexyl group, a cyclopropyl group, a cyclohexyl group, and a4-methylcyclohexyl group.

Further, an alkoxy group represented by R_(s4) and R_(s5) is preferablyan alkoxy group having 1 to 20 carbon atoms. Examples thereof include amethoxy group, an ethoxy group, a butoxy group, a dodecyloxy group, aneicosyloxy group, an i-propoxy group, a t-butoxy group, a t-pentyloxygroup, an i-butoxy group, a 1,1-dimethylbutoxy group, a 2-ethylhexyloxygroup, a cyclopropyloxy group, and a cyclohexyloxy group.

The above-mentioned alkyl, cycloalkyl, and alkoxy groups may have asubstituent(s) (e.g., a chlorine atom, a hydroxyl group, analkoxycarbonyl group, an acyl group, and an acylamino group).

Among the high boiling point organic solvents represented by the formula[S-II], the compounds represented by the following formula [S-II′] arepreferable.

R_(s4) in formula [S-II′] has the same meaning as R_(s4) in formula[S-II]. R_(s5) in formula [S-II′] represents a hydrogen atom or has thesame meaning as R_(s5) in formula [S-II]. R_(s5)′ in formula [S-II′] hasthe same meaning as R_(s5) in formula [S-II]. s1′ represents an integerof 1 to 3. In the case where R_(s5)′ is 2 or more, the plural R_(s5)'smay be the same or different, and R_(s5)′ and R_(s5) may be the same ordifferent.

In the formula [S-II′], more preferable is the case where R_(s5) is ahydrogen atom, an alkyl group, or a halogen atom (e.g., chlorine atom orbromine atom).

R_(s4), R_(s5), and R_(s5)′ are selected based on the nondiffusibilityand solubility of the compound, and on the effects to shift thewavelength at maximum (peak) absorption of the color-formed dye. Thetotal of the carbon atoms of the groups represented by R_(s4), R_(s5),and R_(s5)′ is preferably 50 or less (preferably 12 to 50) and morepreferably 32 or less (preferably 12 to 32).

Hereinafter, specific examples of the high boiling point organic solventrepresented by formula [S-II] will be shown, but the present inventionshould not be considered to be limited thereto.

The high boiling point organic solvents represented by the formula[S-II] can be synthesized according to the methods in, for example, U.S.Pat. No. 2,835,579, JP-B-52-27534, and the like.

Next, the high boiling point organic solvent, which is represented bythe formula [S-III], will be explained.

In the formula [S-III], R_(s6) represents a linking group having noaromatic group, which linking group is bivalent in the case where sm is2, trivalent in the case where sm is 3, tetravalent in the case where smis 4, and pentavalent in the case where sm is 5.

The linking group may be straight-chain, branched, or cyclic. Thelinking group may also have an unsaturated bond.

Examples of the linking group include an alkylidene group, acycloalkylidene group, an alkylene group, a cycloalkylene group, analkenylene group, a cycloalkenylene group, an alkanetriyl group, acycloalkanetriyl group, an alkenetriyl group, a cycloalkenetriyl group,an alkanetetrayl group, a cycloalkanetetrayl group, an alkenetetraylgroup, a cycloalkenetetrayl group, an alkanepentayl group, acycloalkanepentayl group, an alkenepentayl group, and acycloalkenepentayl group. Specific examples of these groups includemethylene, ethylidene, isopropylidene, cyclohexylidene, ethylene,ethylethylene, propylene, trimethylene, tetramethylene, pentamethylene,hexamethylene, heptamethylene, octamethylene, undecamethylene,2,2-dimethyltrimethylene, 1,2-cyclohexylene, 1,4-cyclohexylene,3,4-epoxycyclohexane-1,2-ylene, 3,8-tricyclo[5.2.1.0^(2,6)]decylene,vinylene, propenylene, 4-cyclohexene-1,2-ylene, 2-pentenylene,4-propyl-2-octenylene, 1,2,3-propanetriyl, 1,2,4-butanetriyl,2-hydroxy-1,2,3-propanetriyl, 2-acetyloxy-1,2,3-propanetriyl,1,5,8-octanetriyl, 1,2,3-propenetriyl, 2-propene-1,2,4-triyl,2,6-octadiene-1,4,8-triyl, 1,2,3,4-butanetetrayl,1,3-propanediyl-2-ylidene, 1,3,5,8-octanetetrayl,1-butene-1,2,3,4-tetrayl, 3-octene-1,3,5,8-tetrayl,1,2,3,4,5-pentanepentayl, 1,2,3,5,6-hexanepentayl,2-pentene-1,2,3,4,5-pentayl, and 3,5-decadiene-1,2,3,9,10-pentayl.

sm represents an integer of 2 to 5, preferably 2 or 3, more preferably2.

In the case where sm is 2 or more, the plural —COOR_(s7)s may be thesame or different.

R_(s7) represents an alkyl group (number of carbon atoms is preferably 1to 20), a cycloalkyl group (number of carbon atoms is preferably 3 to20), an alkenyl group (number of carbon atoms is preferably 2 to 20), oran alkynyl group (number of carbon atoms is preferably 2 to 20), eachhaving 20 or less carbon atoms. Specific examples of R_(s7) arestraight-chain or branched alkyl groups or cycloalkyl groups such asmethyl, ethyl, n-butyl, pentyl, neopentyl, hexyl, cyclohexyl, octenyl,2-ethylhexyl, decyl, dodecyl, hexadecyl, and eicosanyl; alkenyl groupssuch as 2-butenyl, 2-pentenyl, 2-nonyl-2-butenyl, and 1,2,5-octadienyl;and alkynyl groups such as 2-propynyl, 2-pentene-4-ynyl, andoctane-5-ynyl. The groups represented by R_(s7) are alkyl groups,preferably.

R_(s6) and R_(s7) may each have a further substituent. Preferredexamples of the substituent include an alkoxy group, an aryloxy group,an epoxy group, a hydroxyl group, an acyloxy group, an aryl group, analkylthio group, an arylthio group, an acyl group, an acylamino group, ahalogen atom and the like, more preferably an alkoxy group (e.g.methoxy, butoxy, butoxyethoxy), an epoxy group, a hydroxyl group, anacyloxy group (e.g. acetyloxy, propionyloxy, cyclohexanoyloxy) and ahalogen atom (e.g. fluorine atom).

Hereinafter, specific examples of the high boiling point organic solventrepresented by formula [S-III] will be shown, but the present inventionshould not be considered to be limited thereto.

Next, the high boiling point organic solvent, which is represented bythe formula (S-IV), will be explained in detail.

In the formula [S-IV], R_(s8) represents a linking group, which linkinggroup is bivalent in the case where sn is 2, trivalent in the case wheresn is 3, tetravalent in the case where sn is 4, and pentavalent in thecase where sn is 5.

The linking group may be straight-chain, branched, or cyclic. Thelinking group may also have an unsaturated bond.

The above liking group is preferably one having no aromatic group.Examples of the linking group include an alkylidene group, acycloalkylidene group, an alkylene group, a cycloalkylene group, analkenylene group, a cycloalkenylene group, an alkanetriyl group, acycloalkanetriyl group, an alkenetriyl group, a cycloalkenetriyl group,an alkanetetrayl group, a cycloalkanetetrayl group, an alkenetetraylgroup, a cycloalkenetetrayl group, an alkanepentayl group, acycloalkanepentayl group, an alkenepentayl group, and acycloalkenepentayl group.

Specific examples of these groups include methylene, ethylidene,isopropylidene, cyclohexylidene, ethylene, ethylethylene, propylene,trimethylene, tetramethylene, pentamethylene, hexamethylene,heptamethylene, octamethylene, undecamethylene,2,2-dimethyltrimethylene, 1,2-cyclohexylene, 1,4-cyclohexylene,3,4-epoxycyclohexane-1,2-ylene, 3,8-tricyclo[5.2.1.0^(2,6)]decylene,vinylene, propenylene, 4-cyclohexene-1,2-ylene, 2-pentenylene,4-propyl-2-octenylene, 1,2,3-propanetriyl, 1,2,4-butanetriyl,2-hydroxy-1,2,3-propanetriyl, 2-acetyloxy-1,2,3-propanetriyl,1,5,8-octanetriyl, 1,2,3-propenetriyl, 2-propene-1,2,4-triyl,2,6-octadiene-1,4,8-triyl, 1,2,3,4-butanetetrayl,1,3-propanediyl-2-ylidene, 1,3,5,8-octanetetrayl,1-butene-1,2,3,4-tetrayl, 3-octene-1,3,5,8-tetrayl,1,2,3,4,5-pentanepentayl, 1,2,3,5,6-hexanepentayl,2-pentene-1,2,3,4,5-pentayl, and 3,5-decadiene-1,2,3,9,10-pentayl.

sn represents an integer of 2 to 5, preferably 2 or 3, more preferably2. In the case where sn is 2 or more, the plural —OCOR_(s9)s may be thesame or different.

R_(s9) represents an alkyl group (number of carbon atoms is preferably 1to 20), a cycloalkyl group (number of carbon atoms is preferably 3 to20), an alkenyl group (number of carbon atoms is preferably 2 to 20), oran alkynyl group (number of carbon atoms is preferably 2 to 20), eachhaving 20 or less carbon atoms. Specific examples of R_(s9) arestraight-chain or branched alkyl groups or cycloalkyl groups such asmethyl, ethyl, n-butyl, pentyl, neopentyl, hexyl, cyclohexyl, octenyl,2-ethylhexyl, decyl, dodecyl, hexadecyl, and elcosanyl; alkenyl groupssuch as 2-butenyl, 2-pentenyl, 2-nonyl-2-butenyl, and 1,2,5-octadienyl;and alkynyl groups such as 2-propynyl, 2-pentene-4-ynyl, andoctane-5-ynyl. The groups represented by R_(s9) are alkyl groups,preferably.

R_(s8) and R_(s9) may each have a further substituent. Preferredexamples of the substituent include an alkoxy group, an aryloxy group,an epoxy group, a hydroxyl group, an acyloxy group, an aryl group, analkylthio group, an arylthio group, an acyl group, an acylamino group, aketone group, a halogen atom and the like, more preferably an alkoxygroup (e.g. methoxy, butoxy, butoxyethoxy), an epoxy group, a hydroxylgroup, an acyloxy group (e.g. acetyloxy, propionyloxy, cyclohexanoyloxy)and a halogen atom (e.g. fluorine atom).

Hereinafter, specific examples of the high boiling point organic solventrepresented by formula [S-IV] will be shown, but the present inventionshould not be considered to be limited thereto.

Next, the high boiling point organic solvent, which is represented bythe formula [S-V], will be explained.

In the formula [S-V], R_(s10), R_(s11), R_(s12), and R_(s13) eachindependently represent a hydrogen atom, an aliphatic group, analiphatic oxycarbonyl group (e.g., dodecyloxycarbonyl,allyloxycarbonyl), an aromatic oxycarbonyl group (e.g.,phenoxycarbonyl), or an carbamoyl group (e.g., tetradecylcarbamoyl,phenyl-methylcarbamoyl), wherein all of R_(s10), R_(s11), R_(s12), andR_(s13) simultaneously do not represent a hydrogen atom, and the totalof the carbon atoms of these groups is 8 to 60. These groups may eachhave a substituent(s).

In formula [S-V], R_(s10) and R_(s11), R_(s12) and R_(s13), or R_(s10)and R_(s12), may bond each other, to form a 5- to 7-membered ring,respectively.

In the formula [S-V], it is preferable that at least one of R_(s10),R_(s11), R_(s12), and R_(s13) is a hydrogen atom and it is morepreferable that two of R_(s10), R_(s11), R_(s12), and R_(s13) are each ahydrogen atom.

In the formula [S-V], it is preferable that at least one of R_(s10),R_(s11), R_(s12) and R_(s13) is an alkyl group substituted with an aryl-or alkyl-ether group, an ester group, or an amido group.

The high boiling point organic solvent, which is used in the presentinvention, preferably in the third embodiment, and which is representedby the formula [S-V], can be synthesized according to the methods in,for example, U.S. Pat. Nos. 4,239,851, 4,540,654.

Hereinafter, specific examples of the high boiling point organic solventrepresented by formula [S-V] will be shown, but the present inventionshould not be considered to be limited thereto.

Next, the high boiling point organic solvent, which is represented bythe formula [S-VI], will be explained.

In the formula [S-VI], R_(s14) represents an aromatic linking groupwhich may have a substituent. sp represents an integer of 3 or more but5 or less and is preferably 3 or 4. Besides, R_(s14) is a trivalentgroup in the case where sp is 3, a tetravalent group in the case wheresp is 4, and a pentavalent group in the case where sp is 5. In the casewhere sp is 2 to 5, the plural —COOR_(s15) groups may be the same ordifferent. R_(s14) is preferably a benzene ring group having a valencyof sp.

R_(s15) represents an alkyl group (the number of carbon atoms ispreferably 1 to 20), a cycloalkyl group (the number of carbon atoms ispreferably 3 to 20), an alkenyl group (the number of carbon atoms ispreferably 2 to 20), or an alkynyl group (the number of carbon atoms ispreferably 2 to 20), each having 20 or less carbon atoms. Specificexamples of R_(s15) are straight-chain or branched alkyl groups orcycloalkyl groups such as methyl, ethyl, n-butyl, pentyl, neopentyl,hexyl, cyclohexyl, octenyl, 2-ethylhexyl, decyl, dodecyl, hexadecyl, andeicosanyl; alkenyl groups such as 2-butenyl, 2-pentenyl,2-nonyl-2-butenyl, and 1,2,5-octadienyl; and alkynyl groups such as2-propynyl, 2-pentene-4-ynyl, and octane-5-ynyl. The group representedby R_(s15) is an alkyl group, preferably.

R_(s15) may further have a substituent. Preferred examples of thesubstituent include an alkoxy group, an aryloxy group, an epoxy group, ahydroxyl group, an acyloxy group, an aryl group, an alkylthio group, anarylthio group, an acyl group, an acylamino group, a halogen atom andthe like, more preferably an alkoxy group (e.g. methoxy, butoxy,butoxyethoxy), an epoxy group, a hydroxyl group, an acyloxy group (e.g.acetyloxy, propionyloxy, cyclohexanoyloxy) and a halogen atom (e.g.fluorine atom).

Hereinafter, specific examples of the high boiling point organic solventrepresented by formula [S-VI] will be shown, but the present inventionshould not be considered to be limited thereto.

The compound represented by the formula [S-VI] can be easilysynthesized, according to, for example, a reaction between an acidhalide of a corresponding carboxylic acid and a corresponding alcohol,or a transesterification reaction between the ester of a correspondingcarboxylic acid and a corresponding alcohol.

The high boiling point organic solvent in the present invention,preferably in the third embodiment means an organic solvent whoseboiling point at 1 atm. is 160° C. or higher.

In the present invention, preferably in the third embodiment, the amountto be used of the high boiling point organic solvent represented by anyone of the formula [S-I] to [S-VI] cannot be specified specifically,because the amount varies depending on the kind and amount to be used ofthe coupler in the present invention. However, the high boiling pointorganic solvent (mass)/coupler (mass) ratio is preferably 0.05 to 20,more preferably 0.1 to 10, and most preferably 0.1 to 3.

In the present invention, preferably in the third embodiment, althoughmany methods can be used as the method of incorporating the coupler foruse in the present invention and the high boiling point organic solventthat can be used in the present invention, preferably in the thirdembodiment into a silver halide emulsion layer, the method preferablycomprises: dissolving, and dispersing the coupler in the presentinvention with the high boiling point organic solvent in the presentinvention, preferably in the third embodiment.

The high boiling point organic solvent according to the presentinvention, preferably to the third embodiment may be used singly or in acombination of two or more thereof. The high boiling point organicsolvent according to the present invention, preferably to the thirdembodiment may be used together with another high boiling point organicsolvent. Further, in order to accelerate the above-mentioneddissolution, a low boiling point organic solvent, and an organic solventmiscible with water can be additionally used.

Examples of the low boiling point organic solvent include ethyl acetate,butyl acetate, cyclohexanone, isobutyl alcohol, methyl ethyl ketone,methyl cellosolve, and the like.

Examples of the organic solvent miscible with water include methanol,ethanol, acetone, phenoxyethanol, tetrahydrofuran, dimethylformamide,and the like.

These low boiling point organic solvent and organic solvent misciblewith water can be removed by such method as washing with water or dryingafter applying.

The organic solvents described above may be used in combination of twoor more thereof.

Next, the compound represented by the formula [ST-I] will be explained.

Examples of the aliphatic groups represented by R₄₀, R₅₀, and R₆₀include an alkyl group having 1 to 32 carbon atoms, an alkenyl grouphaving 2 to 32 carbon atoms, an alkynyl group having 2 to 32 carbonatoms, a cycloalkyl group having 3 to 32 carbon atoms, and acycloalkenyl group having 3 to 32 carbon atoms. The alkyl group, alkenylgroup, and alkynyl group may be straight-chain or branched ones. Thesealiphatic groups include those having a substituent(s).

Examples of the aromatic group represented by R₄₀, R₅₀, and R₆₀ includearyl groups (e.g., phenyl and the like), aromatic heterocyclic groups(e.g., pyridyl, furyl, and the like), and the like. These aromaticgroups include those having a substituent(s).

Preferably R₄₀, R₅₀, and R₆₀ are each an alkyl group or an aryl group,wherein R₄₀, R₅₀, and R₆₀ may be the same or different. The total numberof the carbon atoms of the groups represented by R₄₀, R₅₀, and R₆₀ ispreferably 6 to 50.

Although the substituent on the aliphatic group or aromatic grouprepresented by R₄₀, R₅₀, and R₆₀ is not particularly limited, preferredexamples of the substituent include an alkoxy group, an aryloxy group,an acyl group, an acyloxy group, an alkoxycarbonyl group, anaryloxycarbonyl group, a carbamoyl group, a sulfamoyl group, anacylamino group, an amino group, and the like.

14, m4, and n4 each independently represent 0 or 1, but all of 14, m4,and n4 simultaneously do not represent 1. That is, at least one of thealiphatic groups or aromatic groups represented by R₄₀, R₅₀, and R₆₀ islinked directly to the phosphorus atom. It is preferable that all of 14,m4, and n4 are 0.

Hereinafter, representative examples of the compound represented byformula [ST-I] will be shown, but the present invention should not beconsidered to be limited thereto.

The compounds represented by the formula [ST-I] include the compoundsdescribed on pages 4 to 5 of JP-A-56-19049.

Some of the compounds represented by the formula [ST-I] are commerciallyavailable. Otherwise, these compounds can be synthesized according tothe methods described in, for example, JP-A-56-19049; U.K. Patent No.694,772; J. Am. Chem. Soc., 79, 6524 (1957); J. Org. Chem., 25, 1000(1960); Org. Synth., 31, 33 (1951), and others.

Next, the compound represented by the formula [ST-II] will be explained.

In the formula [ST-II], example of the groups represented by R_(A) andR_(B) include an alkyl group having 1 to 32 carbon atoms, an alkenyl oralkynyl group having 2 to 32 carbon atoms, and a cycloalkyl orcycloalkenyl group having 3 to 12 carbon atoms. The alkyl group, alkenylgroup, and alkynyl group may be straight-chain or branched ones. Thesealiphatic groups include those having a substituent(s).

The aryl groups represented by R_(A) and R_(B) are preferably phenylgroups, which include those having a substituent(s).

The heterocyclic groups represented by R_(A) and R_(B) are preferably 5-to 7-membered ones, which may be condensed with another ring, andinclude those having a substituent(s).

The alkoxy groups represented by R_(A) and R_(B) include those having asubstituent(s). Examples of the alkoxy group include 2-ethoxyethoxy,pentadecyloxy, 2-dodecyloxyethoxy, phenethyloxyethoxy, and the like.

The aryloxy group is preferably a phenyloxy group, wherein the arylnuclei may have a substituent(s). Examples of the aryloxy group includephenoxy, p-t-butylphenoxy, m-pentadecylphenoxy, and the like.

Further, the heterocycloxy group is preferably those having a 5- to7-membered heterocycle which may have a substituent(s). Examples of theheterocycloxy group include 3,4,5,6-tetrahydropyranyl-2-oxy,1-phenyltetrazole-5-oxy, and the like.

Among the compounds represented by the formula [ST-II], particularlypreferred compounds are those represented by the following formula[ST-II′].RE—NHSO₂—RF  Formula [ST-II′]

In the formula [ST-II′], RE and RF each independently represent an alkylgroup or an aryl group each of which may have a substituent(s). It ispreferable that at least one of RE and RF is an aryl group, and it ismore preferable that RE and RF each are an aryl group, a phenyl group inparticular. In the case where RE is a phenyl group, it is particularlypreferable that the Hammett OP constant of the substituent in apara-position with respect to a sulfonamide group is −0.4 or more.

The alkyl group and the aryl group represented by RE and RF have thesame meanings as the alkyl group and the aryl group represented by R_(A)and R_(B) in the formula [ST-II], respectively.

Further, the compounds represented by the formula [ST-II] may form apolymer greater than a dimer at R_(A) or R_(B). Further, R_(A) and R_(B)may bond together to form a 5- or 6-membered ring.

Still further, the total of the carbon atoms of the compound representedby the formula [ST-II] is preferably 8 or more, and more preferably 12or more. The total of the carbon atoms is preferably 60 or less in anycase.

Hereinafter, representative examples of the compound represented byformula [ST-II] will be shown, but the present invention should not beconsidered to be limited thereto. R_(A)—NHSO₂—R_(B) Compound No. R_(A)R_(B) ST-II-1

ST-II-2

ST-II-3

ST-II-4

ST-II-5

ST-II-6

ST-II-7

ST-II-8

ST-II-9

ST-II-10

ST-II-11

ST-II-12

ST-II-13

ST-II-14

ST-II-15

ST-II-16

ST-II-17

ST-II-18

ST-II-19

ST-II-20

ST-II-21

ST-II-22

ST-II-23

ST-II-24

ST-II-25

ST-II-26

ST-II-27

ST-II-28

ST-II-29

ST-II-30

ST-II-31

ST-II-32

ST-II-33

ST-II-34

ST-II-35

ST-II-36

ST-II-37

ST-II-38

ST-II-39

ST-II-40

ST-II-41

ST-II-42

ST-II-43

ST-II-44

ST-II-45

ST-II-46

ST-II-47

ST-II-48

ST-II-49

—C₁₆H₃₃ ST-II-50

—C₁₆H₃₃ ST-II-51

—C₁₆H₃₃ ST-II-52

—C₁₆H₃₃ ST-II-53

—C₁₆H₃₃ ST-II-54

—C₁₆H₃₃ ST-II-55

—C₈H₁₇ ST-II-56

ST-II-57

—C₃H₇(i) ST-II-58 C₈H₁₇—

ST-II-59

ST-II-60 CH₃—

ST-II-61 Cl(CH₂)₂—

ST-II-62 CF₃CF₂—

ST-II-63

ST-II-64 C₈H₁₇—

ST-II-65 C₁₂H₂₅—

ST-II-66

ST-II-67

ST-II-68

ST-II-69

ST-II-70

ST-II-71

ST-II-72

ST-II-73

ST-II-74

ST-II-75

ST-II-76

ST-II-77

ST-II-78

ST-II-79

ST-II-80

ST-II-81

ST-II-82

ST-II-83

ST-II-84

ST-II-85 C₈H₁₇—

ST-II-86

ST-II-87 C₈H₁₇— —C(CH₃)₃ ST-II-88 CCl₃CH₂— —C₁₆H₃₃ ST-II-89

ST-II-90 H—

ST-II-91

ST-II-92 CF₃CH═CH—

ST-II-93

ST-II-94 HOCH₂CH₂C≡C—

ST-II-95

—C₁₈H₃₇ ST-II-96

ST-II-97 C₄H₉CO—

ST-II-98 C₁₀H₂₁NHCO—

ST-II-99

—OC₂H₅ ST-II-100

ST-II-101

ST-II-102

—NH₂ ST-II-103

ST-II-104

ST-II-105

ST-II-106

ST-II-107

ST-II-108

ST-II-109

ST-II-110

ST-II-111

ST-II-112

ST-II-113

ST-II-114

ST-II-115

ST-II-116

ST-II-117

ST-II-118

ST-II-119

ST-II-120

ST-II-121

ST-II-122

The compound represented by the formula [ST-II] can be synthesizedaccording to a conventionally known method such as the method describedin JP-A-62-178258.

The amount to be used of the compound represented by the formula [ST-II]is preferably 5 to 50 mol %, more preferably 10 to 300 mol %, to theamount of the coupler.

Part of the compounds represented by the formula [ST-II] are describedin JP-A-57-76543, JP-A-57-179842, JP-A-58-1139, JP-A-62-178258, andothers.

Next, the compound represented by the formula [ST-III] will beexplained.

Examples of the bivalent group represented by J′ include an alkylenegroup, and alkenylene group, a cycloalkylene group, an arylene group, aheterocyclic group, and a -J″-NH— group (wherein J″ represents anarylene group). These groups may have a substituent(s).

It is preferable that the alkyl group, cycloalkyl group, aryl group,alkenyl group, alkynyl group, and cycloalkenyl group, which are eachrepresented by Y, have carbon atoms in the range of 1 to 32. These alkylgroup, alkenyl group, and alkynyl group may each be a straight-chaingroup or a branched group. Further, these groups include those having asubstituent(s).

Further, the heterocyclic group represented by Y is preferably anitrogen-containing heterocyclic group.

Examples thereof include such groups as pyrrolyl, pyrazolyl, imidazolyl,pyridyl, pyrrolinyl, imidazolidinyl, imidazolinyl, piperazinyl, andpiperidinyl. These heterocyclic groups include those having asubstituent(s).

Hereinafter, representative examples of the compound represented byformula [ST-III] will be shown, but the present invention should not beconsidered to be limited thereto.

Among the compounds represented by the formula [ST-IV], particularlypreferred compounds in the present invention, preferably in the thirdembodiment are those represented by any of the following formulae[ST-IV-I] to [ST-IV-IV].

R′₅₀ to R′₅₉ in the above formulae each have the same meanings as R₅₁and R₅₂ in the formula [ST-IV].

m5 represents an integer of 0 to 6 and n5 represents an integer of 1 to10.

Further, in the formula [ST-IV-III], any two selected from R′₅₄ to R′₅₇may bond together to form a ring.

Further, the compounds described in JP-A-62-257152, JP-A-62-257153, andJP-A-62-272247 can also be used preferably in the present invention,preferably in the third embodiment.

Hereinafter, representative examples of the compound represented byformula [ST-IV] will be shown, but the present invention should not beconsidered to be limited thereto.

No. R₅₁ R₅₂ m₅ ST-IV-1 —C₆H₁₃ —C₆H₁₃ 1 ST-IV-2 —C₆H₁₃ —C₆H₁₃ 2 ST-IV-3—C₆H₁₃ —C₆H₁₃ 3 ST-IV-4 —C₆H₁₃ —C₆H₁₃ 0 ST-IV-5

1 ST-IV-6

2 ST-IV-7

3 ST-IV-8

0 ST-IV-9

1 ST-IV-10

2 ST-IV-11 —COCH₃ —COCH₃ 1 ST-IV-12 —COCH₃ —COCH₃ 2 ST-IV-13 —COCH₃—COCH₃ 3 ST-IV-14 —COCH₃ —COCH₃ 4 ST-IV-15 —C₆H₁₃ —COCH₃ 1 ST-IV-16—C₆H₁₃ —COCH₃ 2 ST-IV-17 —C₆H₁₃ —COCH₃ 3 ST-IV-18 —C₂H₅

1 ST-IV-19 —C₂H₅

2 ST-IV-20 —C₆H₁₃

1 ST-IV-21 —C₆H₁₃

2 ST-IV-22

1 ST-IV-23

2 ST-IV-24

1 ST-IV-25

2 ST-IV-26 —CH₂COOC₄H₉

0 ST-IV-27 —CH₂COOC₄H₉

1 ST-IV-28 —C₄H₉ —C₄H₉ 2 ST-IV-29 —C₄H₉ —C₄H₉ 4 ST-IV-30 —C₄H₉ —C₄H₉ 6ST-IV-31

1 ST-IV-32

2 ST-IV-33 —C₁₂H₂₅ —C₁₂H₂₅ 0 ST-IV-34 —C₁₂H₂₅ —C₁₂H₂₅ 1 ST-IV-35 —C₂H₅

0 ST-IV-36 —C₈H₁₇

0 ST-IV-37 —C₈H₁₇

0 ST-IV-38 —C₁₂H₂₅

0 ST-IV-39 —C₂H₅

0

No. R₅₁ R₅₂ n₅ ST-IV-40 —C₄H₉ —C₄H₉ 3 ST-IV-41 —C₄H₉ —C₄H₉ 4 ST-IV-42—C₄H₉ —C₄H₉ 5 ST-IV-43 —C₄H₉ —C₄H₉ 6 ST-IV-44 —C₈H₁₇ —C₄H₉ 4 ST-IV-45—COCH₃ —COCH₃ 1 ST-IV-46 —COCH₃ —COCH₃ 3 ST-IV-47 —COCH₃ —COCH₃ 4ST-IV-48 —COCH₃ —COCH₃ 6 ST-IV-49

3 ST-IV-50

4 ST-IV-51

5 ST-IV-52

6 ST-IV-53

3 ST-IV-54

4 ST-IV-55

—COCH₃ 3 ST-IV-56 —C₆H₁₃ —COCH₃ 3 ST-IV-57 —C₁₂H₂₅ —C₁₂H₂₅ 3 ST-IV-58—C₁₂H₂₅ —C₁₂H₂₅ 4

No. R₅₁ R₅₂ R₅₂′ R₅₂′ ST-IV-59 —C₄H₉ —C₄H₉ —C₄H₉ —C₄H₉ ST-IV-60 —C₆H₁₃—C₆H₁₃ —C₆H₁₃ —C₆H₁₃ ST-IV-61 —C₈H₁₇ —C₈H₁₇ —C₈H₁₇ —C₈H₁₇ ST-IV-62—COCH₃ —COCH₃ —COCH₃ —COCH₃ ST-IV-63 —COC₃H₇(t) —COC₃H₇(t) —COC₃H₇(t)—COC₃H₇(t) ST-IV-64 —COC₄H₉ —COC₄H₉ —COC₄H₉ —COC₄H₉ ST-IV-65

ST-IV-66

ST-IV-67 —COCH₃ —COCH₃ —C₄H₉ —C₄H₉ ST-IV-68 —COCH₃ —C₄H₉ —C₄H₉ —C₄H₉

ST-IV-69

ST-IV-70

No. R₅₁ R₅₂ ST-IV-71 —COC₆H₁₃ —COC₆H₁₃ ST-IV-72

ST-IV-73 —COC₈H₁₇ —COC₈H₁₇ ST-IV-74 —COC₈H₁₇ —C₆H₁₃ ST-IV-75 —COC₈H₁₇—COC₆H₁₃ ST-IV-76 —COC₇H₁₅ —COC₇H₁₅ ST-IV-77 —COC₇H₁₅ —C₈H₁₇ ST-IV-78—C₁₂H₂₅ —C₁₂H₂₅ ST-IV-79 —C₁₂H₂₅

ST-IV-80 —COC₁₂H₂₅

Some of the compounds represented by the formula [ST-IV] arecommercially available. Otherwise, these compounds can be synthesizedaccording to the methods described in, for example, JP-B-56-1616,JP-A-62-257152, JP-A-62-272247 and others.

Next, the compound represented by the formula [ST-VI] will be explained.

R₅₄ represents a hydrophobic group in which the total of the carbonatoms is 10 or more (preferably 10 to 50 and more preferably 10 to 32),and which is preferably the aliphatic or aromatic group, more preferablythe aliphatic group, as exemplified as R₄₀, R₅₀, and R₆₀ in the formula[ST-I]. Y₅₄ represents a monovalent organic group having an alcoholichydroxyl group. Y₅₄ is preferably a monovalent organic group representedby the following formula (AL).Y₅₅-(L₅₅)m₅₅₋  Formula (AL)

In the formula, Y₅₅ represents a group to give a compound formed byeliminating a hydrogen atom from one of the plural hydroxyl groupscontained in a polyhydric alcohol. L₅₅ represents a bivalent linkinggroup. m₅₅ represents 0 or 1.

Preferred examples of the polyhydric alcohol, which becomes the grouprepresented by Y₅₅ by the elimination of a hydrogen atom, are glycerin,polyglycerin, pentaerythritol, trimethylol propane, neopentyl glycol,sorbitan, sorbide, sorbit, saccharides, and the like. The bivalentlinking groups represented by L are preferably —C(═O)— and —SO₂—.

A preferred compound in the other form of the compound represented bythe formula [ST-V] is a compound in which R₅₄ is an aliphatic grouphaving 12 or more carbon atoms (preferably an alkyl or alkenyl grouphaving 12 to 32 carbon atoms) and Y₅₄ is an OH group.

Hereinafter, representative examples of the compound represented byformula [ST-V] will be shown, but the present invention should not beconsidered to be limited thereto.

The compound, which is represented by any one of the formulae [ST-I] to[ST-V] in the present invention, preferably in the third embodiment, ispreferably used in a layer which is incorporated with a yellowdye-forming coupler represented by the formula (I) or (II) in thepresent invention. It is preferable that the range of the amounts to beused of the compound, which is represented by any one of the formula[ST-I] to [ST-V] in the present invention, preferably in the thirdembodiment, is the same as the previously described range of the amountsto be used of the compound represented by any one of the formula [S-I]to [S-VI]. Although it is preferable that the compound, which isrepresented by any one of the formula [ST-I] to [ST-V] in the presentinvention, preferably in the third embodiment, is used also as a highboiling point organic solvent, it is more preferable that this compoundis used in combination with a high boiling point organic solvent in thepresent invention, preferably in the third embodiment, or another highboiling point organic solvent (preferably in combination with a highboiling point organic solvent in the present invention, preferably inthe third embodiment).

Next, the water-insoluble but organic solvent-soluble homopolymer orcopolymer, which can be used in the present invention, preferably in thethird embodiment, will be explained in detail.

Although various polymers can be used as the water-insoluble but organicsolvent-soluble homopolymer or copolymer (hereinafter referred to as thecopolymer for use in the present invention, preferably the thirdembodiment), for example, the following polymers can be used preferably.

(1) Vinyl-Based Polymers and Copolymers

The monomers, which are to be used for the formation of the vinyl-basedpolymers and copolymers relating to the present invention, preferablythe third embodiment, are specifically listed below:

Acrylates: for example, methyl acrylate, ethyl acrylate, n-propylacrylate, isopropyl acrylate, n-butyl acrylate, tert-butyl acrylate,isobutyl acrylate, sec-butyl acrylate, amyl acrylate, hexyl acrylate,2-ethylhexyl acrylate, octyl acrylate, tert-octyl acrylate,2-chloroethyl acrylate, 2-bromoethyl acrylate, 4-chlorobutyl acrylate,cyanoethyl acrylate, 2-acetoxyethyl acrylate, dimethylaminoethylacrylate, benzyl acrylate, methoxybenzyl acrylate, 2-chlorocyclohexylacrylate, cyclohexyl acrylate, furfuryl acrylate, tetrahydrofurfurylacrylate, phenyl acrylate, 5-hydroxypentyl acrylate,2,2-dimethyl-3-hydroxypropyl acrylate, 2-methoxyethyl acrylate,3-methoxybutyl acrylate, 2-ethoxyethyl acrylate, 2-iso-propoxyethylacrylate, 2-butoxyethyl acrylate, 2-(2-methoxyethoxy)ethyl acrylate,2-(2-butoxy)ethyl acrylate, w-methoxypolyethyleneglycol acrylate (numberof moles added n=9), 1-bromo-2-methoxyethyl acrylate,1,1-dichloro-2-ethoxyethyl acrylate;

Methacrylates: for example, methyl methacrylate, ethyl methacrylate,n-propyl methacrylate, isopropyl methacrylate, n-butyl methacrylate,tert-butyl methacrylate, isobutyl methacrylate, sec-butyl methacrylate,amyl methacrylate, hexyl methacrylate, cyclohexyl methacrylate, benzylmethacrylate, chlorobenzyl methacrylate, octyl methacrylate, sulfopropylmethacrylate, N-ethyl-N-phenylaminoethyl methacrylate,2-(3-phenylpropyloxy)ethyl methacrylate, dimethylaminophenoxyethylmethacrylate, furfuryl methacrylate, tetrahydrofurfuryl methacrylate,phenyl methacrylate, cresyl methacrylate, naphthyl methacrylate,2-hydroxyethyl methacrylate, 4-hydroxybutyl methacrylate,triethyleneglycol monomethacrylate, dipropyleneglycol monomethacrylate,2-methoxyethyl methacrylate, 3-methoxybutyl methacrylate, 2-acetoxyethylmethacrylate, 2-acetoacetoxyethyl methacrylate, 2-ethoxyethylmethacrylate, 2-iso-propoxyethyl methacrylate, 2-butoxyethylmethacrylate, 2-(2-methoxyethoxy)ethyl methacrylate,2-(2-ethoxyethoxy)ethyl methacrylate, 2-(2-butoxyethoxy)ethylmethacrylate, ω-methoxypolyethyleneglycol methacrylate (number of molesadded n=6);

Vinyl esters: for example, vinyl acetate, vinyl propionate, vinylbutylate, vinyl isobutylate, vinyl caproate, vinyl chloroacetate, vinylmethoxy acetate, vinylphenyl acetate, vinyl benzoate, vinyl salicylate;

Acrylamides: for example, acrylamide, methylacrylamide, ethylacrylamide,propylacrylamide, butylacrylamide, tert-butylacrylamide,cyclohexylacrylamide, benzylacrylamide, hydroxymethylacrylamide,methoxyethylacrylamide, dimethylaminoethylacrylamide, phenylacrylamide,dimethylacrylamide, diethylacrylamide, cyanoethylacrylamide,N-(2-acetoacetoxyethyl)acrylamide, diacetoneacrylamide;

Methacrylamides: for example, methacrylamide, methylmethacrylamide,ethylmethacrylamide, propylmethacrylamide, butylmethacrylamide,tert-butylmethacrylamide, cyclohexylmethacrylamide,benzylmethacrylamide, hydroxymethylmethacrylamide,methoxyethylmethacrylamide, dimethylaminoethylmethacrylamide,phenylmethacrylamide, dimethylmethacrylamide, diethylmethacrylamide,cyanoethylmethacrylamide, N-(2-acetoacetoxyethyl)methacrylamide;

Olefins: for example, dicyclopentadiene, ethylene, propylene, 1-butene,1-pentene, vinyl chloride, vinylidene chloride, isoprene, chloroprene,butadiene, 2,3-dimethylbutadiene;

Styrenes: for example, styrene, methylstyrene, dimethylstyrene,trimethylstyrene, ethylstyrene, isopropylstyrene, chloromethylstyrene,methoxystyrene, chlorostyrene, dichlorostyrene, bromostyrene, methylester of vinylbenzoic acid;

Crotonates: for example, butyl crotonate, hexyl crotonate; Diesters ofitaconic acid: for example, dimethyl itaconate, diethyl itaconate,dibutyl itaconate; Diesters of maleic acid: for example, diethylmaleate, dimethyl maleate, dibutyl maleate;

Diesters of fumaric acid: for example, diethyl fumarate, dimethylfumarate, dibutyl fumarate; and the like.

Examples of other monomers are as follows: allyl compounds: for example,allyl acetate, allyl caproate, allyl laurate, allyl benzoate; vinylethers: for example, methyl vinyl ether, butyl vinyl ether, hexyl vinylether, methoxyethyl vinyl ether, dimethylaminoethyl vinyl ether; vinylketones: for example, methyl vinyl ketone, phenyl vinyl ketone,methoxyethyl vinyl ketone; vinyl-heterocyclic compounds: for example,vinylpyridine, N-vinylimidazole, N-vinyloxazolidone, N-vinyltriazole,N-vinylpyrrolidone; gycidyl esters: for example, glycidyl acrylate,glycidyl methacrylate; unsaturated nitriles: for example, acrylonitrile,methacrylonitrile; and the like.

The polymer that can be used in the present invention, preferably in thethird embodiment, may be a homopolymer of any of the above-mentionedmonomers or, if necessary, a copolymer of two or more of theabove-mentioned monomers. Although the polymer that can be used in thepresent invention, preferably in the third embodiment, may comprise amonomer having an acid group to an extent that the polymer is not madewater-soluble (the content of such a monomer is preferably 20% or less),the polymer that is entirely free of such a monomer is preferable.Examples of the monomer having an acid group include acrylic acid;methacrylic acid; itaconic acid; maleic acid; monoalkyl itaconate (e.g.,monomethyl itaconate); monoalkyl maleate (e.g., monomethyl maleate);citraconic acid; styrenesulfonic acid; vinylbenzylsulfonic acid;acryloyloxyalkylsulfonic acid (e.g., acryloyloxymethylsulfonic acid);methacryloyloxyalkylsulfonic acid (e.g., methacryloyloxymethylsulfonicacid, methacryloyloxyethylsulfonic acid, methacryloyloxypropylsulfonicacid); acrylamidealkylsulfonic acid (e.g.,2-acrylamide-2-methylethanesulfonic acid,2-acrylamide-2-methylpropanesulfonic acid,2-acrylamide-2-methylbutanesulfonic acid); methacrylamidealkylsulfonicacid (e.g., 2-methacrylamide-2-methylethanesulfonic acid,2-methacrylamide-2-methylpropanesulfonic acid,2-methacrylamide-2-methylbutanesulfonic acid); acryloyloxyalkylphosphate (e.g., acryloyloxyethyl phosphate,3-acryloyloxypropyl-2-phosphate); methacryloyloxyalkyl phosphate (e.g.,methacryloyloxyethyl phosphate, 3-methacryloyloxypropyl-2-phosphate);and the like.

These monomers having an acid group(s) may be a salt(s) of alkali metal(e.g., Na, K) or of an ammonium ion.

The monomers, which form the polymers that can be used in the presentinvention, preferably in the third embodiment, are preferablyacrylate-based monomers, methacrylate-based monomers, acrylamide-basedmonomers, and methacrylamide-based monomers.

The polymers, which comprise the above-mentioned monomers, can beobtained by a solution polymerization process, a bulk polymerizationprocess, a suspension polymerization process, or a latex polymerizationprocess. Examples of the initiators, which can be used in theabove-mentioned polymerization processes, include a water-solublepolymerization initiator and a lipophilic polymerization initiator.

Examples of the water-soluble polymerization initiator that can be usedinclude persulfates such as potassium persulfate, ammonium persulfate,and sodium persulfate; water-soluble azo compounds such as sodium4,4′-azobis-4-cyanovalerate and 2,2′-azobis(2-amidinopropane)hydrochloride; and hydrogen peroxide.

Examples of the lipophilic polymerization initiator include lipophilicazo compounds such as azobisisobutyronitrile,2,2′-azobis(2,4-dimethylvaleronitrile),2,2′-azobis(4-methoxy-2,4-dimethylvaleronitrile),1,1′-azobis(cyclohexanone-1-carbonitrile),2,2′-azobisdimethylisobutyrate, and 2,2′-azobisdiethylisobutyrate aswell as benzoyl peroxide, lauryl peroxide, diisopropylperoxydicarbonate, and di-tert-butylperoxide.

(2) As a polyhydric alcohol for a polyester resin obtainable by thecondensation between a polyhydric alcohol and a polybasic acid, glycolsrepresented by HO—R_(a)—OH (wherein R_(a) represents a hydrocarbon,particularly an aliphatic hydrocarbon, having 2 to about 12 carbonatoms) or a polyalkylene glycol are effective. As the polybasic acid,polybasic acids represented by HOOC—R_(b)—COOH (wherein R_(b) representsa simple linkage or a hydrocarbon having 1 to 12 carbon atoms) areeffective.

Specific examples of the polyhydric alcohol include ethylene glycol,diethylene glycol, triethylene glycol, 1,2-propylene glycol,1,3-propylene glycol, trimethylol propane, 1,4-butanediol,isobutylenediol, 1,5-pentanediol, neopentyl glycol, 1,6-hexanediol,1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol,1,11-undecanediol, 1,12-dodecanediol, 1,13-tridecanediol,1,14-tetradecanediol, glycerin, diglycerin, triglycerin,1-methylglycerin, erythrite, mannite, sorbit, and the like.

Specific examples of the polybasic include oxalic acid, succinic acid,glutaric acid, adipic acid, pimelic acid, cork acid, azelaic acid,sebacic acid, nonanedicarboxylic acid, decanedicarboxylic acid,undecanedicarboxylic acid, dodecanedicarboxylic acid, fumaric acid,maleic acid, itaconic acid, citraconic acid, phthalic acid, isophthalicacid, terephthalic acid, tetrachlorophthalic acid, methaconic acid,isopimelic acid, a cyclopentadiene/maleic anhydride adduct, arosin/maleic anhydride adduct, and the like.

(3) Polyesters Obtainable by a Ring-Opening Polymerization Process

These polyesters are obtained from β-propiolactone, ε-caprolactone,dimethylpropiolactone, and the like.

(4) Others

Examples of other polymers include a polycarbonate resin obtained by apolycondensation reaction between a glycol or dihydric phenol and acarbonic ester or phosgene; a polyurethane resin obtained by apolyaddition reaction between a polyhydric alcohol and a polyvalentisocyanate; and a polyamide resin obtained from a polyvalent amine and apolybasic acid.

Although the number average molecular weight of the polymer that can beused in the present invention, preferably in the third embodiment, isnot particularly limited, it is preferably 200,000 or less, morepreferably 800 or more but 100,000 or less.

Hereinafter, specific examples of the polymer that can be used in thepresent invention, preferably in the third embodiment, will be shown,but the present invention should not be considered to be limited thereto(the compositions of the polymers in parentheses are indicated in termsof mass ratio).

-   P-1) poly(N-sec-butylacrylamide)-   P-2) poly(N-tert-butylacrylamide)-   P-3) diacetoneacrylamide/methyl methacrylate copolymer (25:75)-   P-4) poly(cyclohexyl methacrylate)-   P-5) N-tert-butylacrylamide/methyl methacrylate copolymer (60:40)-   P-6) poly(N,N-dimethylacrylamide)-   P-7) poly(tert-butyl methacrylate)-   P-8) poly(vinyl acetate)-   P-9) poly(vinyl propionate)-   P-10) poly(methyl methacrylate)-   P-11) poly(ethyl methacrylate)-   P-12) poly(ethyl acrylate)-   P-13) vinyl acetate-vinyl alcohol copolymer (90:10)-   P-14) poly(n-butyl acrylate)-   P-1S) poly(n-butyl methacrylate)-   P-16) poly(isobutyl methacrylate)-   P-17) poly(isopropyl methacrylate)-   P-18) poly(octyl acrylate)-   P-19) n-butyl acrylate/acrylamide copolymer (95:5)-   P-20) stearyl methacrylate/acrylic acid copolymer (90:10)-   P-21) methyl methacrylate/vinyl chloride copolymer (70:30)-   P-22) methyl methacrylate/styrene copolymer (90:10)-   P-23) methyl methacrylate/ethyl acrylate copolymer (50:50)-   P-24) n-butyl methacrylate/methyl methacrylate/styrene:copolymer    (50:20:30)-   P-25) vinyl acetate/acrylamide copolymer (85:15)-   P-26) vinyl chloride/vinyl acetate copolymer (65:35)-   P-27) methyl methacrylate/acrylonitrile copolymer (65:35)-   P-28) n-butyl methacrylate/pentyl methacrylate/N-vinyl-2-pyrrolidone    copolymer (38:38:24)-   P-29) methyl methacrylate/n-butyl methacrylate/isobutyl    methacrylate/acrylic acid copolymer (37:29:25:9)-   P-30) n-butyl methacrylate/acrylic acid copolymer (95:5)-   P-31) methyl methacrylate/acrylic acid copolymer (95:5)-   P-32) benzyl methacrylate/acrylic acid copolymer (93:7)-   P-33) n-butyl methacrylate/methyl methacrylate/benzyl    methacrylate/acrylic acid copolymer (35:35:25:5)-   P-34) n-butyl methacrylate/methyl methacrylate/benzyl methacrylate    copolymer (40:30:30)-   P-35) diacetoneacrylamide/methyl methacrylate copolymer (50:50)-   P-36) methyl vinyl ketone/isobutyl methacrylate copolymer (55:45)-   P-37) ethyl methacrylate/n-butyl acrylate copolymer (70:30)-   P-38) diacetoneacrylamide/n-butyl acrylate copolymer (60:40)-   P-39) methyl methacrylate/stearyl methacrylate/diacetoneacrylamide    copolymer (40:40:20)-   P-40) n-butyl acrylate/stearyl methacrylate/diacetoneacrylamide    copolymer (70:20:10)-   P-41) stearyl methacrylate/methyl methacrylate/acrylic acid    copolymer (50:40:10)-   P-42) methyl methacrylate/styrene/vinylsulfonamide:copolymer    (70:20:10)-   P-43) methyl methacrylate/phenyl vinyl ketone copolymer (70:30)-   P-44) n-butyl acrylate/methyl methacrylate/n-butyl methacrylate    copolymer (35:35:30)-   P-45) n-butyl methacrylate/N-vinyl-2-pyrrolidone copolymer (90:10)-   P-46) poly(pentyl acrylate)-   P-47) cyclohexyl methacrylate/methyl methacrylate/n-propyl    methacrylate copolymer (37:29:34)-   P-48) poly(pentyl methacrylate)-   P-49) methyl methacrylate/n-butyl methacrylate copolymer (65:35)-   P-50) vinyl acetate/vinyl propionate copolymer (75:25)-   P-51) n-butyl methacrylate/sodium 3-acryloxybutane-1-sulfonate    copolymer (97:3)-   P-52) n-butyl methacrylate/methyl methacrylate/acrylamide:copolymer    (35:35:30)-   P-53) n-butyl methacrylate/methyl methacrylate/vinyl chloride    copolymer (37:36:27)-   P-54) n-butyl methacrylate/styrene copolymer (82:18)-   P-55) tert-butyl methacrylate/methyl methacrylate:copolymer (70:30)-   P-56) poly(N-tert-butylmethacrylamide)-   P-57) N-tert-butylacrylamide/methylphenyl methacrylate:copolymer    (60:40)-   P-58) methyl methacrylate/acrylonitrile copolymer (70:30)-   P-59) methyl methacrylate/methyl vinyl ketone copolymer (28:72)-   P-60) methyl methacrylate/styrene copolymer (75:25)-   P-61) methyl methacrylate/hexyl methacrylate copolymer (70:30)-   P-62) butyl methacrylate/acrylic acid copolymer (85:15)-   P-63) methyl methacrylate/acrylic acid copolymer (80:20)-   P-64) methyl methacrylate/acrylic acid copolymer (98:2)-   P-65) methyl methacrylate/N-vinyl-2-pyrrolidone copolymer (90:10)-   P-66; n-butyl methacrylate/vinyl chloride copolymer (90:10)-   P-67) n-butyl methacrylate/styrene copolymer (70:30)-   P-68) 1,4-butanediaol/adipic acid polyester-   P-69) ethylene glycol/sebacic acid polyester-   P-70) poly(caprolactam)-   P-71) poly(propiolactam)-   P-72) poly(dimethylpropiolactone)-   P-73) N-tert-butylacrylamide/dimethylaminoethylaramide:copolymer    (85:15)-   P-74) N-tert-butylmethacrylamide/vinylpyridine copolymer (95:5)-   P-75) diethyl maleate/n-butyl acrylate copolymer (65:35)-   P-76) N-tert-butylacrylamide/2-methoxyethyl acrylate copolymer    155:45)

The polymer of still another preferable mode that can be used in thepresent invention, preferably in the third embodiment, is a polymersubstantially insoluble in water which comprises as a constituentelement thereof a monomer unit having at least one aromatic group, andwhich has a number average molecular weight of 2,000 or less. The numberaverage molecular weight is preferably 200 or more but less than 2,000,and more preferably 200 or more but 1,000 or less. The polymer that canbe used in the present invention, preferably in the third embodiment,may be a so-called homopolymer composed of one kind of monomer unit, ora copolymer composed of two kinds or more of monomer units. In the caseof a copolymer, it preferably comprises the monomer unit having thearomatic group, according to the present invention, preferably to thethird embodiment, in a proportion of 20% or more of the weightcomposition of the copolymer. The polymer structure is not particularlylimited in so far as the above-mentioned condition is fulfilled.Examples of the polymer having the preferred polymer structure include apolymer whose constituent element is styrene, β-methylstyrene,P-methylstyrene, or a monomer having a substituent on the benzene ringof such a monomer; a polymer whose constituent element is an aromaticacrylamide, an aromatic methacrylamide, an aromatic acrylate, or anaromatic methacrylate. Examples of the aromatic group include a phenylgroup, a naphthyl group, a benzyl group, a biphenyl group, and the like.These aromatic groups may have a substituent(s) such as an alkyl group,a halogen atom, and the like. In the case of a copolymer, comonomerslisted, for example, in JP-A-63-264748 can be used preferably. From theviewpoints of availability of raw materials and stability of an emulsionwith the lapse of time, a polymer derived from styrene, α-methylstyreneor β-methylstyrene is preferable.Hereinafter specific examples of the polymer for use in the presentinvention, preferably in the third embodiment, will be shown, but thepresent invention should not be considered to be limited thereto. In thespecific examples, l, m, and n may take any value only if the numberaverage molecular weight of the polymer is less than 2,000.

In the present invention, preferably in the third embodiment, thehomopolymer or copolymer used in the present invention, preferably inthe third embodiment, is used preferably as a dispersion to be presenttogether with the coupler for use in the present invention in lipophilicparticles. The dispersion can be obtained by dissolving the coupler andat least one of the homopolymer or copolymer used in the presentinvention, preferably in the third embodiment, in a high boiling pointorganic solvent substantially insoluble in water and dispersing theresulting solution by emulsification in a hydrophilic protectivecolloid.

Herein, the high-boiling-point organic solvent substantially insolublein water is a compound, which has a melting point of 100° C. or belowand a boiling point of 140° C. or above, and which is not miscible withwater. Examples thereof include phenol derivatives, esters such asphthalic esters and phosphoric esters, amides of organic acids,carbamates, ketones, and others. These are described, for example, inU.S. Pat. Nos. 2,322,027, 2,353,262, 2,533,514, 2,801,170, 2,801,171,2,835,579, 2,852,383, 2,870,012, 2,991,171, 3,287,134, 3,554,755,3,676,137, 3,676,142, 3,700,454, 3,748,141, 3,779,765, and 3,837,863.

For the formation of lipophilic particles by dispersing the couplerrelated to the present invention and the compound related to the presentinvention, preferably to the third embodiment, by emulsification in ahydrophilic protective colloid, the dispersing operation is carried outby means of a mixer, a homogenizer, a colloid mill, a flow jet mixer, anultrasonic apparatus, or the like, using a dispersing aid such as asurfactant. A process for removing a low boiling point organic solventmay be employed simultaneously with the dispersing operation.

An aqueous solution of gelatin is preferably used as the hydrophilicprotective colloid. The average particle diameter of the lipophilicparticles is preferably 0.04 to 2 μm, and more preferably 0.06 to 0.4μm. The particle diameter can be measured by Coulter model N4 (tradename) manufactured by U.K. Coulter Corp., or the like.

In the above-described procedure, the mixing ratio of the coupler,homopolymer or copolymer, high boiling point organic solvent, and anauxiliary solvent such as a low boiling point organic solvent or anorganic solvent miscible with water, may be selected such that thesolution, which is formed by dissolving the coupler, homopolymer orcopolymer, and high boiling point organic solvent in the auxiliarysolvent, has a viscosity suitable for being easily dispersed in thehydrophilic protective colloid. Although the ratio cannot be definedunqualifiedly because it varies depending on the solubility of thecoupler and the kind or degree of polymerization of the polymer to beused, an example of the ratio of the polymer to the coupler (mass ratio)is generally 1:10 to 5:1, and preferably 1:3 to 2:1.

In the case where a polymer insoluble in water and a high boiling pointorganic solvent are used in combination, the ratio of the high boilingpoint organic solvent to the coupler (mass ratio) is generally 1:20 to5:1, and preferably 1:10 to 2:1. The ratio of the low boiling pointorganic solvent to the polymer (mass ratio) is generally 1:10 to 10:1,and preferably 1:4 to 5:1.

It is preferable that the homopolymer or copolymer is not a polyestermade from an aliphatic dicarboxylic acid and an aliphatic diol, in thecase of a yellow dye-forming coupler represented by the formula (I)wherein Q is —C(—R11)=C(—R12)-CO— (where R11 and R12 are groups thatbond together to form a 5- to 7-membered ring together with the —C═C—,or each independently represent a hydrogen atom or a substituent).

In the present invention, preferably in the third embodiment, among thecompounds represented by any one of the formulas [S-I] to [S-VI] or[ST-I] to [ST-V] and the water-insoluble homopolymers or copolymers,which are used together with the yellow dye-forming coupler representedby the formula (I) or (II) in the present invention, preferred compoundsor preferred combinations of these compounds are as follows.

In the present invention, preferably in the third embodiment, from thestandpoint of stability at the time of rapid processing, preferredcompounds or preferred combinations of these compounds are a combinationof a compound represented by the formula [S-II] and a compoundrepresented by the formula [S-I], a compound represented by the formula[S-IV], a combination of a compound represented by the formula [ST-II]and a compound represented by the formula [S-I], a combination of acompound represented by the formula [ST-III] and a compound representedby the formula [S-I], and a combination of a compound represented by theformula [ST-V] and a compound represented by the formula [S-I].

Besides, from the standpoint of stability in an unexposed state,preferred compounds or preferred combinations of these compounds are acompound represented by the formula [S-I], a compound represented by theformula [S-III], a compound represented by the formula [S-V], a compoundrepresented by the formula [S-VI], a combination of a compoundrepresented by the formula [ST-IV] and a compound represented by theformula [S-I], and a combination of a compound represented by theformula [S-I] and A water-insoluble polymer used in the presentinvention, preferably in the third embodiment.

Particularly preferable are a compound represented by the formula [S-V],a compound represented by the formula [S-VI], and a combination of acompound represented by the formula [S-III] and a compound representedby the formula [S-I].

Further, from the standpoint of fastness to humidity and heat, preferredcompounds are a compound represented by the formula [S-I], a compoundrepresented by the formula [S-V], a compound represented by the formula[S-VI], and a compound represented by the formula [S-I].

As the cyan dye-forming coupler (herein also referred to as “cyancoupler”) which can be used in the present invention, preferably in thethird and fourth embodiments, pyrrolotriazole-series couplers arepreferably used, and more specifically, couplers represented by any offormulae (1) and (II) in JP-A-5-313324 and couplers represented byformula (I) in JP-A-6-347960 are preferred. Exemplified couplersdescribed in these publications are particularly preferred. Further,phenol-series or naphthol-series cyan couplers are also preferred. Forexample, cyan couplers represented by formula (ADF) described inJP-A-10-333297 are preferred. As preferable cyan couplers other than theforegoing cyan couplers, mention can be made of: pyrroloazole-type cyancouplers described in European Patent Nos. 0 488 248 and 0 491 197 (A1),2,5-diacylamino phenol couplers described in U.S. Pat. No. 5,888,716,pyrazoloazole-type cyan couplers having an electron-withdrawing group ora group bonding via hydrogen bond at the 6-position, as described inU.S. Pat. Nos. 4,873,183 and 4,916,051, and particularlypyrazoloazole-type cyan couplers having a carbamoyl group at the6-position, as described in JP-A-8-171185, JP-A-8-311360 andJP-A-8-339060.

In addition, use can be made of diphenyllmidazole-series cyan couplersdescribed in JP-A-2-33144; as well as 3-hydroxypyridine-series cyancouplers (particularly a 2-equivalent coupler formed by allowing a4-equivalent coupler of a coupler (42), to have a chlorine splitting-offgroup, and couplers (6) and (9), enumerated as specific examples areparticularly preferable) described in European Patent 0333185 A2; cyclicactive methylene-series cyan couplers (particularly couplers 3, 8, and34 enumerated as specific examples are particularly preferable)described in JP-A-64-32260; pyrrolopyrazole-type cyan couplers describedin European Patent No. 0456226 A1; and pyrroloimidazole-type cyancouplers described in European Patent No. 0484909.

Among these cyan couplers, pyrroloazole-series cyan couplers representedby formula (I) described in JP-A-11-282138 are particularly preferred.The descriptions of the paragraph Nos. 0012 to 0059 includingexemplified cyan couplers (1) to (47) of the above JP-A-11-282138 can beentirely applied to the present invention, preferably to the thirdembodiment, and therefore the descriptions are preferably incorporatedby reference in the present specification.

Next, the relative coupling rate in the present invention, preferably inthe fourth embodiment, will be described.

Oxidation of p-phenylenediamine (hereinafter, abbreviated as “PPD”) withsilver halide is a process that takes place at the outset of thecolor-developing process and this is a rate-limiting process. The PPD isconverted into quinonediimine (hereinafter, abbreviated as “QDI⁺) whensubjected to two-electron oxidation. On the other hand, a couplerpresent in an oil drop is dissociated into an anion (hereinafter,abbreviated as “Cp⁻”), which forms a color-forming dye (hereinafter,abbreviated as “Dye”) upon reaction with the QDI⁺.

The relative coupling rate can be calculated, by making the compound Aco-exist in the color-development reaction system and measuring thedegree of a decrease in the rate of the color development reaction dueto competition of the reaction between the compound A (hereinafter,abbreviated as “A-”) and the QDI⁺.

It is assumed that the coupling reaction proceeds as follows.QDI⁺+Cp⁻→Dye Reaction rate constant k_(Cp)QDI⁺+A⁻→QDI-A Reaction rate constant k_(A)QDI⁺→Deactivation/efflux, etc. Reaction rate constant k_(d)

In the above, A⁻ represents a dissociate form of the compound A, andQDI-A represents a coupling product from the compound A and the QDI.

The dye production yield Φin the system in which the compound A coexistsis represented by the equation (1) described below.Φ=k_(Cp)/(k _(Cp) +k _(d) +k _(A) [A])  (1)

By taking an inverse number of the equation (1), the equation (2) belowis obtained. $\begin{matrix}\begin{matrix}{{1/\phi} = {1 + {\left( {k_{d} + {k_{A}\lbrack A\rbrack}} \right)/k_{C_{p}}}}} \\{= {\left( {1 + {k_{d}/k_{Cp}}} \right) + {{k_{A}\lbrack A\rbrack}/k_{C_{p}}}}}\end{matrix} & (2)\end{matrix}$

In the equation (2) above, [A] is the concentration (mol/l) of thecompound A that exists in the system (color developer). Note that, asshown above, the color developer has a pH of 10.05, so that all themolecules of the compound A exist as A⁻ and hence [A⁻] is equal to [A].Therefore, [A] is used in place of [A⁻] herein.

In the equation (2), 1/4′ is plotted as a function of [A], and aninverse number of the inclination (k_(Cp)/k_(A)) of the straight lineobtained by the plotting is defined as the relative coupling rate.

The dye production yield Φ can be experimentally obtained, by plottingthe number of moles of color forming dye vs. the amount of developedsilver at varied concentrations [A] of the compound A, and determiningthe initial gradient tan θ thereof.

Since the relative coupling rate obtained by the above-mentionedexperimental technique varies depending on the color-developmentprocessing, the composition of the processing solution and theprocessing conditions for the color-development processing on which therelative coupling rate calculation in the present invention, preferablyin the fourth embodiment, is based are shown below. Triethanolamine 8.1g/l Potassium chloride 2.9 g/l Potassium bromide 0.02 g/l Potassiumhydrogen carbonate 4.8 g/l Potassium sulfite 0.1 g/lN-ethyl-N-(β-methanesulfonamidoethyl)-3-methyl-4- 4.5 g/l aminoaniline3/2 sulfate monohydrate Potassium carbonate 18.4 g/l Addition of waterto make 1,000 ml pH (25° C./adjusted with potassium hydroxide and 10.05sulfuric acid Temperature 35° C. Processing time 45 seconds

Thereafter, bleach-fixing and washing (rinsing) are performed fordesilvering. If desilvering is performed ordinarily, no influence isgiven on the calculation of relative coupling rates. For example, bleachfixing and rinsing in standard RA-4 [Eastman Kodak] processing orcolor-development processing B described in Example 4-3 in the presentspecification (preferably, the latter method) are carried out and acolored sample after drying is measured as described below.

Specifically, 1.0 g/l or less of the compound A is optionally added tothe above-mentioned color-development processing solution (preferably,with adjusting the addition amount of the compound A such that a densityregion from the maximum color density given by the above-mentionedcolor-developer without addition of the compound A to the density of anunexposed portion can be divided at approximately regular intervals, andwith plotting at five or more measuring points, preferably 20 measuringpoints), and the concentration of a dye obtained from the coupler to bemeasured is measured with respect to the addition amount, followed bycalculating a relative coupling rate, k (k_(Cp)/K_(A)), to the compoundA.

The sample of which the relative coupling rate is obtained has amultilayer structure having at least one yellow color-forminglight-sensitive silver halide emulsion layer, at least one magentacolor-forming light-sensitive silver halide emulsion layer, and at leastone cyan color-forming light-sensitive silver halide emulsion layer, andat least one non-light-sensitive and non-color-forming hydrophiliccolloid layer. The relative coupling rate of the yellow color-formingcoupler can be calculated by exposing it to blue light, the relativecoupling rate of the magenta color-forming coupler can be calculated byexposing it to green light, and the relative coupling rate of the cyancolor-forming coupler can be calculated by exposing it to red light. Theyellow color-forming light-sensitive silver halide emulsion layer, themagenta color-forming light-sensitive silver halide emulsion layer, andthe cyan color-forming light-sensitive silver halide emulsion layer eachpreferably contain a color-forming coupler and a photosensitive silverhalide emulsion in the same layer, and each color-forming layer ispreferably coated one by one in view of reducing the thickness of layer.

Note that although the ratio of the number of moles of coloring dye tothe amount of developed silver may be obtained by any method, the amountof dye in the case of a reflective support can be obtained by extractingthe sample that developed a color.

Also, plural couplers may be contained in each color-formingcoupler-containing light-sensitive silver halide emulsion layer. In suchcase, the number of moles of produced dye can be obtained from waveformseparation of extracted dyes or liquid-liquid chromatography. Theaverage relative coupling rate, ka, is calculated by weight averagingwith a compositional mole fraction.

The average relative coupling rate, kar′, of the couplers in eachphotographic light-sensitive material is obtained as follows. That is,Sample 4-001 described in Example 4-1 in the present specification isexposed to blue light, and the average relative coupling rate, ka, whenthe yellow coupler forms color is taken as 1.0, and a relative value tothis is defined as the average relative coupling rate, kar, defined inthe present invention, preferably in the fourth embodiment.

Note that the term “average” is used because when plural couplers arecontained in the same photosensitive silver halide emulsion layer, theaverage relative coupling rate, ka, is weight averaged with thecompositional mole fraction as described above, but the case where onlyone kind of coupler is contained in the emulsion layer should also beincluded in “average” according to the above-mentioned calculationdefinition.

For example, the average relative coupling rates, ka, of color paperscurrently on the market are cyan 1.23, magenta 0.51, and yellow 1.01 forFuji Color Ever Beauty Paper for Laser (trade name) manufactured by FujiPhoto Film Co., Ltd., cyan 0.99, magenta 0.45, and yellow 1.48 for aproduct manufactured by a company B, and cyan 0.95, magenta 0.35, andyellow 0.91 for a product manufactured by a company C. These do not meetthe definition in the present invention, preferably in the fourthembodiment.

A preferred range of the average relative coupling rate, kar, is 0.6 ormore and 2.0 or less, more preferably 0.7 or more and 1.8 or less, stillmore preferably 0.7 or more and 1.5 or less, for all the color-formingcoupler-containing silver halide emulsion layers. The average relativecoupling rate, kar, outside the above-mentioned range is not preferable.If the average relative coupling rate, kar, is higher than the rangedefined in the present invention, preferably in the fourth embodiment,it is necessary to design the thickness of an intermediate layer forpreventing color mixing thicker in order to maintain color separability,although color-forming property is enhanced. This deteriorates rapidhigh-productivity processing suitability, and at the same time,deteriorates bleach stain or stain due to the remaining developingagent. If the average relative coupling rate, kar, is lower than therange defined in the present invention, preferably in the fourthembodiment, the silver coating amount or coupler coating amount must beincreased in order to increase color density, which deteriorates rapidhigh-productivity processing suitability and at the same time tends tocause adverse affects such as blix fading.

For balancing the average relative coupling rates, kar, it is preferredthat the layer in which the color-forming coupler has the maximumaverage relative coupling rate kar, among the color-forming couplerscontained in the color-forming photosensitive silver halide emulsionlayers, be positioned in the middle of the three color-formingphotosensitive silver halide emulsion layers.

The silver halide emulsion contained in the yellow color-formingblue-sensitive silver halide emulsion layer preferably has a relativelyhigh sensitivity as compared with the green-sensitive silver halideemulsion and red-sensitive silver halide emulsion, in consideration ofyellow mask of a negative or spectroscopic characteristics of halogenthat is the source at the time of exposure. For this purpose, the sidelength of the grains in the blue-sensitive emulsion is greater than thatof the grains in other layers. Further, the generally known molarextinction coefficient of the coloring dye formed by a yellow coupler islow as compared with those of the coloring dyes formed by the magentacoupler and the cyan coupler, so that increasing yellow coupler coatingamount is accompanied by an increasing coating amount of theblue-sensitive emulsion.

The yellow color-forming blue-sensitive layer is disadvantageous ascompared with other layers when taking into consideration the resistanceto pressure applied from the surface of the photosensitive material,such as scratching, and it is preferably positioned on a side closer tothe support. More preferably, the yellow color-forming blue-sensitivelayer is positioned closest to the support among the silver halideemulsion layers. Most preferably, it is positioned in the positionclosest to the support among all the layers.

In the present invention, preferably in the fourth embodiment, apreferred total silver coating amount is 0.25 g/m² to 0.50 g/m², morepreferably 0.25 g/m² to 0.45 g/m², still more preferably 0.25 g/m² to0.40 g/m².

In the silver halide color photographic light-sensitive materialaccording to the present invention, preferably to the fourth embodiment,gelatin is generally used as a hydrophilic binder. Other hydrophiliccolloids of gelatin derivatives, graft copolymers of gelatin with otherpolymers, proteins other than gelatin, sugar derivatives, cellulosederivatives, synthetic hydrophilic polymeric substances such ashomopolymers and copolymers may be used in combination with gelatin, ifnecessary. The gelatin that can be used in the silver halide colorphotographic light-sensitive material of the present invention,preferably of the fourth embodiment, may be any one of lime-processedgelatin and acid-processed gelatin. Alternatively, it may be gelatinproduced by using any one of bovine bone, bovine skin, and porcine skinas a raw material. Lime-processed gelatin from bovine bone or porcineskin as a raw material is preferred.

In the present invention, preferably in the fourth embodiment, the totalamount of hydrophilic binder contained in the photosensitive silverhalide emulsion layer and the non-photosensitive hydrophilic colloidlayer from the support to the hydrophilic colloid layer remotest fromthe support (on the side where the silver halide emulsion layer(s) isprovided) is generally 5.7 g/m² or less and 4.0 g/m² or more, preferably5.7 g/m² or less and 4.5 g/m or more, more preferably 5.5 g/m² or lessand 5.0 g/m² or more. If the amount of hydrophilic binder is too large,the effects of the present invention, preferably of the fourthembodiment, cannot be sufficiently exhibited, due to deterioration ofthe rapid processability for color-development processing, deteriorationdue to blix fading, deterioration of rapid processability for rinsingstep, and the like. On the other hand, if the amount of the hydrophilicbinder is too small, harmful affection due to insufficient filmstrength, such as pressure-induced fog streak, tends to occur, which isnot preferable.

The water-swelling rate in the present invention, preferably in thefourth embodiment, is that on the side where silver halide emulsionlayers are coated on the support, measured under the environment of 25°C. and relative humidity of 55%, which means the water-swelling ratewhen immersed in water of 35° C. The water-swelling rate is preferably200% or more and 300% or less, more preferably 220% or more and 280% orless. Outside the preferred range of the water-swelling rate, rapidprocessability may be lost in some cases.

The film thickness in the present invention, preferably in the fourthembodiment, is preferably 5.0 μm or more and 7.7 μm or less, morepreferably 5.0 μm or more and 7.0 μm or less, still more preferably 5.0μm or more and 6.5 μm or less.

The effects of the present invention, preferably of the fourthembodiment, tends to be more easily exhibited, under the conditionswhere reciprocity law failure occurs at the time of high illuminanceexposure and where silver development in a shadow portion is difficultto occur. However, at low illuminance exposure, similar effects can beobtained.

The present invention, preferably the fourth embodiment, will bedescribed in more detail based on examples referred to hereinbelow, butunless otherwise specified, the present invention should not beconsidered to be limited thereto.

Hereinafter, silver halide color photographic light-sensitive materialof the present invention, preferably of the fourth embodiment, isexplained below.

In the present invention, preferably in the fourth embodiment, a silverhalide color photosensitive material (hereinafter, sometimes referred tosimply as “photosensitive material”) which has, on a support, at leastone silver halide emulsion layer containing a yellow dye-formingcoupler, at least one silver halide emulsion layer containing a magentadye-forming coupler, and at least one silver halide emulsion layercontaining a cyan dye-forming coupler, is preferably used.

In the present invention, preferably in the fourth embodiment, thesilver halide emulsion layer containing a yellow dye-forming couplerfunctions as a yellow color-forming layer, the silver halide emulsionlayer containing a magenta dye-forming coupler functions as a magentacolor-forming layer, and the silver halide emulsion layer containing acyan dye-forming coupler functions as a cyan color-forming layer.Preferably, the silver halide emulsions contained in the yellowcolor-forming layer, the magenta color-forming layer, and the cyancolor-forming layer may have photosensitivities to mutually differentwavelength regions (for example, light in a blue region, light in agreen region and light in a red region).

The photosensitive material of the present invention, preferably of thefourth embodiment, has at least one non-photosensitive,non-color-forming hydrophilic colloid layer, besides the above-mentionedyellow color-forming layer, magenta color-forming layer and cyancolor-forming layer. As such hydrophilic colloid layer, as will bedescribed later, an antihalation layer, an intermediate layer, anultraviolet ray absorbing layer, a protective layer, a colored layer,and the like may be mentioned.

Herein, the silver halide photographic light-sensitive materialpreferable in the present invention, more preferably in the fourthembodiment is explained below in detail.

The silver halide grains in the silver halide emulsion for use in thepresent invention, preferably in the fourth embodiment, are notparticularly limited in their grain shape, but the silver halide grainsare preferably composed of cubic or tetradecahedral crystal grainssubstantially having a {100} plane (each of the grains may have a roundapex and a plane of a higher order); octahedral crystal grains; andtabular grains having an aspect ratio of 2 or more whose main face is ofa {100} plane or {111} plane. The aspect ratio is defined as the valueobtained by dividing the diameter of a circle corresponding to thecircle having the same area as a projected area of an individual grainby the thickness of the grain. In the present invention, preferably inthe fourth embodiment, cubic or tetradecahedral grains are morepreferable.

The silver halide emulsion which can be used in the present invention,preferably in the fourth embodiment, generally contains silver chloridein a silver chloride content of 95 mol % or more. It is more preferablefor rapid processing suitability to use the silver halide emulsionhaving a silver chloride content of 96 mole % or greater.

Further, the silver halide emulsion for use in the present invention,preferably in the fourth embodiment, preferably contains silver bromideand/or silver iodide. The content of the silver bromide is preferably0.1 to 7 mole %, more preferably 0.5 to 5 mole %, in view of highcontrast and excellent latent image stability. The content of the silveriodide is preferably 0.02 to 1 mole %, more preferably 0.05 to 0.50 mole%, most preferably 0.07 to 0.40 mole %, in view of high contrast andhigh sensitivity under high illumination intensity exposure.

The silver halide emulsion for use in the present invention, preferablyin the fourth embodiment, is preferably a silver iodobromochlorideemulsion, more preferably a silver iodobromochloride emulsion having ahalogen composition described above.

The silver halide grains in the silver halide emulsion for use in thepresent invention, preferably in the fourth embodiment, preferably havea silver bromide-containing phase and/or a silver iodide-containingphase. Herein, a region where the content of silver bromide is higherthan that in other (surrounding) regions will be referred to as a silverbromide-containing phase, and likewise, a region where the content ofsilver iodide is higher than that in other regions will be referred toas a silver iodide-containing phase. The halogen compositions of thesilver bromide-containing phase or the silver iodide-containing phaseand of its periphery may vary either continuously or drastically. Such asilver bromide-containing phase or a silver iodide-containing phase mayform a layer which has an approximately constant concentration and has acertain width at a certain portion in the grain, or it may form amaximum point having no spread. The localized silver bromide content inthe silver bromide-containing phase is preferably 5 mole % or more, morepreferably from 10 to 80 mole %, and most preferably from 15 to 50 mole%. The localized silver iodide content in the silver iodide-containingphase is preferably 0.3 mole % or more, more preferably from 0.5 to 8mole %, and most preferably from 1 to 5 mole %. Such silver bromide- orsilver iodide-containing phase may be present in plural numbers in layerform, within the grain. In this case, the phases may have differentsilver bromide or silver iodide contents from each other. The silverhalide grains for use in the present invention, preferably in the fourthembodiment, have at least one of the silver bromide-containing phase andsilver iodide-containing phase, and preferably contain both of at leastone silver bromide-containing phase and at least one silveriodide-containing phase.

The silver bromide-containing phase or silver iodide-containing phase inthe silver halide emulsion preferably used in the present invention,preferably in the fourth embodiment, preferably exists in a layer stateso that it surrounds the silver halide grain. One preferred embodimentis that the silver bromide-containing phase or the silveriodide-containing phase formed in the layer form so as to surround thegrain center has a uniform concentration distribution in thecircumferential direction of the grain, in each phase. However, in thesilver bromide-containing phase or silver iodide-containing phase formedin the layer form so as to surround the grain center, there may be themaximum point or the minimum point of the silver bromide or silveriodide concentration, in the circumferential direction of the grain tohave a concentration distribution. For example, when a grain has asilver bromide-containing phase or silver iodide-containing phase formedin the layer form so as to surround the grain center in the vicinity ofa surface of the grain, the silver bromide or silver iodideconcentration of a corner portion or an edge of the grain can bedifferent from that of a main surface of the grain. Further, aside froma silver bromide-containing phase or a silver iodide-containing phaseformed in a layer form so as to surround the grain center, anothersilver bromide-containing phase or silver iodide-containing phase thatexists in complete isolation at a specific portion of the surface of thegrain, and does not surround the grain center, may exist.

When a silver halide emulsion grain for use in the present invention,preferably in the fourth embodiment, has a silver bromide-containingphase, the silver bromide-containing phase is preferably formed in alayer form so as to have a maximum point of silver bromide concentrationinside the grain. Likewise, when the silver halide emulsion grain foruse in the present invention, preferably in the fourth embodiment, has asilver iodide-containing phase, the silver iodide-containing phase ispreferably formed in a layer form so as to form a maximum point ofsilver iodide concentration at the surface of the grain. Such a silverbromide-containing phase or silver iodide-containing phase isconstituted preferably with a silver amount of 3% to 30% of the grainvolume, and more preferably with a silver amount of 3% to 15%, in themeaning to increase the local concentration with a less silver bromideor silver iodide content.

The silver halide emulsion grain for use in the present invention,preferably in the fourth embodiment, preferably contains both a silverbromide-containing phase and a silver iodide-containing phase. In thismode, the silver bromide-containing phase and the silveriodide-containing phase may exist either at the same place in the grainor at different places thereof. However, it is preferred that they existat different places, in a point that the control of grain formation maybecome easy. Further, a silver bromide-containing phase may containsilver iodide. Alternatively, a silver iodide-containing phase maycontain silver bromide. In general, an iodide added during formation ofhigh silver chloride grains is liable to ooze to the surface of thegrain more than a bromide, so that the silver iodide-containing phase isliable to be formed at the vicinity of the surface of the grain.Accordingly, when a silver bromide-containing phase and a silveriodide-containing phase exist at different places in a grain, it ispreferred that the silver bromide-containing phase is formed moreinternally than the silver iodide-containing phase. In such a case,another silver bromide-containing phase may be provided further outsidethe silver iodide-containing phase in the vicinity of the surface of thegrain.

A silver bromide or silver iodide content in the silver halide emulsionpreferably used in the present invention, preferably in the fourthembodiment, increases with the silver bromide-containing phase or silveriodide-containing phase is being formed inside a grain. This causes thesilver chloride content to decrease to more than necessary, resulting inthe possibility of impairing rapid processing suitability. Accordingly,for putting together these functions for controlling photographicactions, in the vicinity of the surface of the grain, it is preferredthat the silver bromide-containing phase and the silveriodide-containing phase are placed adjacent to each other. From thesepoints, it is preferred that the silver bromide-containing phase isformed at any of the position ranging from 50% to 100% of the grainvolume measured from the inside, and that the silver iodide-containingphase is formed at any of the position ranging from 85% to 100% of thegrain volume measured from the inside. Further, it is more preferredthat the silver bromide-containing phase is formed at any of theposition ranging from 70% to 95% of the grain volume measured from theinside, and that the silver iodide-containing phase is formed at any ofthe position ranging from 90% to 100% of the grain volume measured fromthe inside.

To a silver halide emulsion grain preferably used in the presentinvention, preferably in the fourth embodiment, bromide ions or iodideions are introduced to make the grain contain silver bromide or silveriodide. In order to introduce bromide ions or iodide ions, a bromide oriodide salt solution may be added alone, or it may be added incombination with both a silver salt solution and a high chloride saltsolution. In the latter case, the bromide or iodide salt solution andthe high chloride salt solution may be added separately or as a mixturesolution of these salts of bromide or iodide and high chloride. Thebromide or iodide salt is generally added in the form of a soluble salt,such as an alkali or alkali earth bromide or iodide salt. Alternatively,bromide or iodide ions may be introduced by cleaving the bromide oriodide ions from an organic molecule, as described in U.S. Pat. No.5,389,508. As another source of bromide or iodide ion, fine silverbromide grains or fine silver iodide grains may be used.

The addition of a bromide salt or iodide salt solution may beconcentrated at one time of grain formation process or may be performedover a certain period of time. For obtaining an emulsion with highsensitivity and low fog, the position of the introduction of an iodideion to a high silver chloride emulsion is restricted. The deeper in theemulsion grain the iodide ion is introduced, the smaller is theincrement of sensitivity. Accordingly, the addition of an iodide saltsolution is preferably started at 50% or outer side of the volume of agrain, more preferably 70% or outer side, and most preferably 85% orouter side. Moreover, the addition of an iodide salt solution ispreferably finished at 98% or inner side of the volume of a grain, morepreferably 96% or inner side. When the addition of an iodide saltsolution is finished at a little inner side of the grain surface,thereby an emulsion having higher sensitivity and lower fog can beobtained.

On the other hand, the addition of a bromide salt solution is preferablystarted at 50% or outer side of the volume of a grain, more preferably70% or outer side of the volume of an emulsion grain.

In this specification, an equivalent spherical diameter of grain means adiameter of a sphere having a volume identical to that of an individualgrain. Preferably, the silver halide emulsion for use in the presentinvention, preferably in the fourth embodiment, is composed of grainshaving a monodisperse particle size distribution.

The variation coefficient of equivalent spherical diameter of all thegrains contained in the silver halide emulsion for use in the presentinvention, preferably in the fourth embodiment, is preferably 20% orless, more preferably 15% or less, and still more preferably 10% orless. The variation coefficient of equivalent spherical diameter isexpressed as a percentage of standard deviation of equivalent sphericaldiameter of each grain to an average of equivalent spherical diameter.In this connection, for the purpose of obtaining broad latitude, it ispreferred that the above-mentioned monodisperse emulsions be used asblended in the same layer or be used in layers formed by multilayercoating.

The equivalent spherical diameter of the grains contained in the silverhalide emulsions that can be used in the present invention, preferablyin the fourth embodiment, is preferably 0.6 μm or less, more preferably0.5 μm or less, and still more preferably 0.4 μm or less. Note that thelower limit of the equivalent spherical diameter of the silver halidegrains, is preferably 0.05 μm, more preferably 0.1 μm. The grain havingan equivalent spherical diameter of 0.6 μm corresponds to a cubic grainhaving a side length of about 0.48 μm, the grain having an equivalentspherical diameter of 0.5 μm corresponds to a cubic grain having a sidelength of about 0.4 μm, and the grain having an equivalent sphericaldiameter of 0.4 μm corresponds to a cubic grain having a side length ofabout 0.32 μm. Among these, in the present invention, preferably in thefourth embodiment, in particular, cubic grains having an average sidelength of 0.10 μm to 0.50 μm are preferred, and those having an averageside length of 0.15 μm to 0.48 μm are more preferred.

The silver halide emulsion grains used in the present invention,preferably in the fourth embodiment, preferably contains (be doped with)iridium, for example, by containing an iridium compound or complex.Iridium preferably is in the form of an iridium complex. As an iridiumcomplex (compound), a six-coordination complex having 6 ligands andcontaining iridium as a central metal is preferable, for uniformlyincorporating iridium in a silver halide crystal. As one preferableembodiment of iridium compound for use in the present invention,preferably in the fourth embodiment, a six-coordination complex havingCl, Br or I as a ligand and containing iridium as a central metal ispreferable. A more preferable example is a six-coordination complex inwhich all six ligands are Cl, Br, or I and which has iridium as acentral metal. In this case, Cl, Br and I may coexist in thesix-coordination complex. It is especially preferable that asix-coordination complex having Cl, Br or I as a ligand and containingiridium as a central metal is contained in a silver bromide-containingphase, in order to obtain a hard gradation in a high illuminationintensity exposure.

Specific examples of the six-coordination complex in which all of 6ligands are Cl, Br or I and iridium is a central metal are shown below,but the iridium compound for use in the present invention is not limitedthereto.

[IrCl₆]²⁻

[IrCl₆]³⁻

[IrBr₆]²⁻

[(IrBr₆]³⁻

[IrI₆]³⁻

As another preferable embodiment of the iridium (compound) that can beused in the present invention, preferably in the fourth embodiment, asix-coordination complex having at least one ligand other than a halogenor a cyan and containing iridium as a central metal, is preferable. Asix-coordination complex having H₂O, OH, O, OCN, thiazole, a substitutedthiazole, thiadiazole, or a substituted thiadiazole as a ligand andcontaining iridium as a central metal is preferable. A six-coordinationcomplex in which at least one ligand is H₂O, OH, O, OCN, thiazole, or asubstituted thiazole and the remaining ligands are Cl, Br or I, andiridium is a central metal, is more preferable. A six-coordinationcomplex in which one or two ligands are 5-methylthiazole,2-chloro-5-fluorothiadiazole or 2-bromo-5-fluorothiadiazole, and theremaining ligands are Cl, Br or I, and iridium is a central metal, ismost preferable.

Specific examples of the six-coordination complex in which at least oneligand is H₂O, OH, O, OCN, thiazole or a substituted thiazole and theremaining ligands are Cl, Br or I, and iridium is a central metal, arelisted below.

However, the iridium compound for use in the present invention is notlimited thereto.

[Ir(H₂O)Cl₅)]²⁻

[Ir(OH)Br₅]³⁻

[Ir(OCN)Cl₅]³⁻

[Ir(thiazole)Cl₅]³⁻

[Ir(5-methylthiazole)Cl₅]²⁻

[Ir(2-chloro-5-fluorothiadiazole)Cl₅]²⁻

[Ir(2-bromo-5-fluorothiadiazole)Cl₅]²⁻

The silver halide emulsion used in the present invention, preferably inthe fourth embodiment, preferably contains, besides the above-mentionediridium complex, a hexacoordination complex containing Fe, Ru, Re or Osas a central metal and containing a CN ligand, such as [Fe(CN)₆]4,[Fe(CN)₆], [Ru(CN)₆], [Re(CN)₆]⁴⁻, and [Os(CN)₆]⁴⁻. It is preferred thatthe silver halide emulsion used in the present invention, preferably inthe fourth embodiment, further contains a pentachloronitrosyl complex ora pentachlorothionitrosyl complex having Ru, Re or Os as a centralmetal, or a hexacoordination complex having Cl, Br or I as a ligand andRh as a central metal. These ligands may be partially aquated.

The above-mentioned metal complexes are anions, and when they form saltswith cations, the counter cations are preferably those that are readilysoluble in water. Specifically, alkali metal ions, such as sodium ion,potassium ion, rubidium ion, cesium ion, and lithium ion; ammonium ion,and alkylammonium ions are preferred. These metal complexes can be usedby dissolving them in water, or in a mixed solvent composed of water andan arbitrary organic solvent miscible with water (for example, alcohols,ethers, glycols, ketones, esters, amides, etc.). These metal complexesare added during formation of silver halide grains in an amount ofpreferably 1×10⁻¹⁰ to 1×10⁻³ mole, more preferably 1×10⁻⁹ to 1×10⁻⁵mole, per mole of silver, although the optimum amount may vary dependingon the kind thereof.

The above-mentioned metal complexes are preferably added directly to thereaction solution at the time of silver halide grain formation, orindirectly to the grain-forming reaction solution via addition to anaqueous halide solution for forming silver halide grains or othersolutions, so that they are doped to the inside of the silver halidegrains. Also, it is preferred that these metal complexes areincorporated into silver halide grains by physically aging fine grainsin which the metal complex has been preliminarily incorporated and thenincorporating such fine grains. Further, these methods may be combinedto have the metal complex contained in the silver halide grains.

In case where these complexes are doped to the inside of the silverhalide grains, they are preferably uniformly distributed in the insideof the grains. On the other hand, as disclosed in JP-A-4-208936,JP-A-2-125245 and JP-A-3-188437, they are also preferably distributedonly in the grain surface layer. Alternatively they are also preferablydistributed only in the inside of the grain while the grain surface iscovered with a layer free from the complex. Further, as disclosed inU.S. Pat. Nos. 5,252,451 and 5,256,530, it is also preferred that thesilver halide grains are subjected to physical ripening in the presenceof fine grains having the complexes incorporated therein to modify thegrain surface phase. Further, these methods may be used in combination.Two or more kinds of the complexes may be incorporated in the inside ofan individual silver halide grain. The composition of halogen at theposition where the above-mentioned complex is contained is notparticularly limited. It is preferred that the hexacoordination complexin which all the six ligands are any of Cl, Br or I and Ir is a centralmetal be contained at the maximum portion on silver bromideconcentration.

In the present invention, preferably in the fourth embodiment, theabove-mentioned gold sensitization together with chalcogen sensitizationcan be performed using the same molecule, and for this purpose amolecule that can release AuCh⁻ can be used. Here, Au represents Au(I)and Ch represents a sulfur atom, a selenium atom, or a tellurium atom.Examples of the molecule that can release AuCh⁻ include a gold compoundrepresented by AuCh-L. Here, L represents a group of atoms that binds toAuCh to constitute the molecule. Further, in addition to Ch-L, one ormore ligands may be coordinated to Au. Specific examples of such acompound include Au(I) salts of thio-sugars (e.g. gold thioglucoses suchas gold thioglucose; gold peracetylthioglucose, gold thiomannose, goldthiogalactose, gold thioarabinose), Au(I) salts of seleno-sugars (e.g.gold peracetylselenoglucose, gold peracetylselenomannose), Au(I) saltsof telluro-sugars, and the like. Here, thio-sugars, seleno-sugars, andtelluro-sugars refer to compounds derived from sugars in which thehydroxyl group at the anomer position of the sugar is replaced by an SHgroup, an SeH group or a TeH group, respectively. The addition amount ofthese compounds may vary widely depending on the case, and generally itis 5×10⁻⁷ to 5×10⁻³ mole, preferably 3×10⁻⁶ to 3×10⁻⁴ mole, per mole ofsilver halide.

To the silver halide emulsion for use in the present invention,preferably in the fourth embodiment, the above-mentioned goldsensitization may be used in combination with another sensitizingmethod, for example, sulfur sensitization, selenium sensitization,tellurium sensitization, reduction sensitization, or noble metalsensitization using a noble metal compound other than gold compounds.The gold sensitization is particularly preferably carried out incombination with sulfur sensitization and/or selenium sensitization.

In the present invention, preferably in the fourth embodiment; thedye-forming coupler (herein, also referred to as “coupler”) is generallyadded to a photographically useful substance or a high-boiling organicsolvent, emulsified and dispersed together with the substance orsolvent, and incorporated into a photosensitive material as a resultingdispersion. This solution (dispersion) is emulsified and dispersed infine grain form, into a hydrophilic colloid, preferably into an aqueousgelatin solution, together with a dispersant which is, for example, asurfactant, by use of a known apparatus such as an ultrasonic device, acolloid mill, a homogenizer, a Manton-Gaulin, or a high-speed dissolver,to obtain a dispersion.

The high-boiling organic solvent that can be used in the presentinvention, preferably in the fourth embodiment, is not particularlylimited, and an ordinary one may be used. Examples of which includethose described in U.S. Pat. No. 2,322,027 and JP-A-7-152129.

Further, when dissolving the coupler, an auxiliary solvent may be usedtogether with the high-boiling point organic solvent. Examples of theauxiliary solvent include acetates of a lower alcohol, such as ethylacetate and butyl acetate; ethyl propionate, secondary butyl acetate,methyl ethyl ketone, methyl isobutyl ketone, β-ethoxyethyl acetate,methyl cellosolve acetate, methyl carbitol acetate, and cyclohexanone.

Further, if necessary, an organic solvent that completely admix withwater, such as methyl alcohol, ethyl alcohol, acetone, tetrahydrofuran,and dimethylformamide, can be additionally used as a part of theauxiliary solvent. These organic solvents can be used in combinationwith two or more.

For the purpose of, for example, improving stability with the lapse oftime at storage in the state of an emulsified dispersion, and improvingstability with the lapse of time and inhibiting the fluctuation ofphotographic property of the end-composition for coating (applying) thatis mixed with an emulsion, if necessary, from the thus-preparedemulsified dispersion, the auxiliary solvent may be removed in itsentirety or part of it, for example, by distillation under reducedpressure, noodle washing, or ultrafiltration.

Preferably, the average particle size of the lipophilic fine-particledispersion obtained in this way is 0.04 to 0.50 μm, more preferably 0.05to 0.30 μm, and most preferably 0.08 to 0.20 μm. The average particlesize can be measured by using Coulter Submicron Particle Analyzer ModelN4 (trade name, manufactured by Coulter Electronics Co.) or the like.

In the oil-in-water droplet dispersing method using a high-boilingorganic solvent, the ratio of the mass of the high-boiling organicsolvent to the total mass of the cyan coupler used may be setarbitrarily, and it is preferably 0.1 or more and 10.0 or less, morepreferably 0.3 or more and 7.0 or less, and most preferably 0.5 or moreand 5.0 or less. Also, the method may be performed without using anyhigh-boiling organic solvent.

Also, a pigment for coloration may be co-emulsified into the emulsionused in the present invention, preferably in the fourth embodiment, inorder to adjust coloration of the white background, or it may coexist inan organic solvent that dissolves the photographically useful compound,such as the coupler, used in the photosensitive material of the presentinvention, preferably of the fourth embodiment, to be co-emulsified,thereby preparing an emulsion.

In the present invention, preferably in the fourth embodiment, the cyancoupler that can be preferably used, may be any coupler that forms acyan dye. Examples thereof include phenol-series cyan couplers,naphthol-series cyan couplers, and heterocyclic couplers. Among these,pyrroloazole couplers are preferred in the present invention, preferablyin the fourth embodiment, more preferably those cyan couplersrepresented by formula (PTA-I) or formula (PTA-II) shown below.

In the above formulae, Zc and Zd each represent —C(R¹³)= or —N═, andwhen one of Zc and Zd represents —C(R¹³)=the other represents —N═. R¹¹and R¹² each independently represent an electron-withdrawing grouphaving a Hammett substituent constant, σp, of 0.2 or more and the sum ofthe σ_(p), values of R¹¹ and R¹² is 0.65 or more. R¹³ represents ahydrogen atom or a substituent. X¹⁰ represents a hydrogen atom or agroup capable of being split-off upon a coupling reaction with anoxidized product of an aromatic primary amine color-developing agent. Yrepresents a hydrogen atom or a group that splits off during the colordevelopment process. The group of R¹¹, R¹², R¹³ or X¹⁰ may be a divalentgroup and form a homopolymer or a copolymer by binding to a dimer or amultimer or a polymer chain.

Among them, a cyan coupler that is more preferably used in view of rapidprocessing suitability, color reproducibility, storage stability of aphotosensitive material in an unexposed state is a cyan couplerrepresented by formula (PTA-III) shown below.

In formula (PTA-III), R¹ and R² each independently represent an alkylgroup or an aryl group, R³, R⁴, and R⁵ each independently represent ahydrogen atom, an alkyl group or an aryl group, Z represents a group ofnon-metal atoms necessary to form a saturated ring, R⁶ represents asubstituent, X²⁰ represents a heterocyclic group, a substituted aminogroup or an aryl group, and Y represents a hydrogen atom or a group thatsplits off during the color development process.

In formula (PTA-III), the alkyl group represented by R¹ to R⁵ is astraight-chain, branched, or cyclic alkyl group having 1 to 36 carbonatoms, preferably a straight-chain, branched, or cyclic alkyl grouphaving 1 to 22 carbon atoms, and especially preferably a straight-chain,or branched alkyl group having 1 to 8 carbon atoms. Specific examplesthereof include methyl, ethyl, n-propyl, isopropyl, t-butyl, t-amyl,t-octyl, decyl, dodecyl, cetyl, stearyl, cyclohexyl, and 2-ethylhexyl.

In formula (PTA-III), the aryl group represented by R¹ to R⁵ is an arylgroup having 6 to 20 carbon atoms, preferably an aryl group having 6 to14 carbon atoms, and especially preferably an aryl group having 6 to 10carbon atoms. Specific examples thereof include phenyl, 1-naphthyl,2-naphthyl, and 2-phenanthryl.

In formula (PTA-III), the group of non-metallic atoms necessary to froma saturated ring, represented by Z, is a group of non-metallic atomsnecessary to form a 5- to 8-membered ring which may have a substituent,and which may be a saturated ring or an unsaturated ring. Thering-forming non-metallic atom may be a carbon atom, an oxygen atom, anitrogen atom, or a sulfur atom. The ring is preferably a 6-memberedsaturated carbon ring, and especially preferably a cyclohexane ringwhich is substituted with an alkyl group having 1 to 24 carbon atoms atthe 4-position thereof.

In formula (PTA-III), examples of the substituent represented by R⁶include, for example, a halogen atom (e.g., a fluorine atom, a chlorineatom, and a bromine atom), an aliphatic group (e.g., a straight-chain orbranched-chain alkyl group, an aralkyl group, an alkenyl group, analkynyl group, a cycloalkyl group, and a cycloalkenyl group, each having1 to 36 carbon atoms, and specifically, for example, methyl, ethyl,propyl, isopropyl, t-butyl, tridecyl, t-amyl, t-octyl,2-methanesulfonylethyl, 3-(3-pentadecylphenoxy)propyl,3-{4-{2-[4-(4-hydroxyphenylsulfonyl)phenoxy]dodecaneamido}-phenyl}propyl,2-ethoxytridecyl, trifluoromethyl, cyclopentyl, and3-(2,4-di-t-amylphenoxy)propyl), an aryl group (e.g., an aryl grouphaving 6 to 36 carbon atoms, for example, phenyl, 4-t-butylphenyl,2,4-di-t-amylphenyl, 4-tetradecaneamidophenyl, 2-methoxyphenyl), aheterocyclic group (e.g., a heterocyclic group having 1 to 36 carbonatoms, for example, 2-furyl, 2-thienyl, 2-pyrimidinyl, and2-benzothiazolyl), a cyano group, a hydroxyl group, a nitro group, acarboxy group, an amino group, an alkoxy group (e.g., a straight-chain,branched-chain or cyclic alkoxy group having 1 to 36 carbon atoms, forexample, methoxy, ethoxy, butoxy, 2-methoxyethoxy, 2-dodecyloxyethoxy,and 2-methanesulfonylethoxy), an aryloxy group (e.g., an aryloxy grouphaving 6 to 36 carbon atoms, for example, phenoxy, 2-methylphenoxy,4-t-butylphenoxy, 3-nitrophenoxy, 3-t-butyloxycarbamoylphenoxy, and3-methoxycarbamoyl), an acylamino group (e.g., an acylamino group having2 to 36 carbon atoms, for example, acetamido, benzamido,tetradecaneamido, 2-(2,4-di-t-amylphenoxy)butaneamido,4-(3-t-butyl-4-hydroxyphenoxy)butaneamido, and2-{4-(4-hydroxyphenylsulfonyl)phenoxy}decaneamido), an alkylamino group(e.g., an alkylamino group having 1 to 36 carbon atoms, for example,methylamino, butylamino, dodecylamino, diethylamino, andmethylbutylamino), an anilino group (e.g., an anilino group having 6 to36 carbon atoms, for example, phenylamino, 2-chloroanilino,2-chloro-5-tetradecaneaminoanilino,2-chloro-5-dodecyloxycarbonylanilino, N-acetylanilino, and2-chloro-5-{2-(3-t-butyl-4-hydroxyphenoxy)dodecaneamido}anilino), aureido group (e.g., a ureido group having 2 to 36 carbon atoms, forexample, phenylureido, methylureido, and N,N-dibutylureido), asulfamoylamino group (e.g., a sulfamoylamino group having 1 to 36 carbonatoms, for example, N,N-dipropylsulfamoylamino andN-methyl-N-decylsulfamoylamino), an alkylthio group (e.g., an alkylthiogroup having 1 to 36 carbon atoms, for example, methylthio, octylthio,tetradecylthio, 2-phenoxyethylthio, 3-phenoxypropylthio, and3-(4-t-butylphenoxy)propylthio), an arylthio group (e.g., an aylthiogroup having 6 to 36 carbon atoms, for example, phenylthio,2-butoxy-5-t-octylphenylthio, 3-pentadecylphenylthio,2-carboxyphenylthio, and 4-tetradecaneamidophenylthio), analkoxycarbonylamino group (e.g., an alkoxycarbonylamino group having 2to 36 carbon atoms, for example, methoxycarbonylamino andtetradecyloxycarbonylamino), a sulfonamido group (e.g., an alkyl- oraryl-sulfonamido group having 1 to 36 carbon atoms, for example,methanesulfonamido, butanesulfonamido, octanesulfonamido,hexadecanesulfonamido, benzenesulfonamido, p-toluenesulfonamido,octadecanesulfonamido, and 2-methoxy-5-t-butylbenzenesulfonamido), acarbamoyl group (e.g., a carbamoyl group having 1 to 36 carbon atoms,for example, N-ethylcarbamoyl, N,N-dibutylcarbamoyl,N-(2-dodecyloxyethyl)carbamoyl, N-methyl-N-dodecylcarbamoyl, andN-{3-(2,4-di-t-amylphenoxy)propyl}carbamoyl), a sulfamoyl group (e.g., asulfamoyl group having 1 to 36 carbon atoms, for example,N-ethylsulfamoyl, N,N-dipropylsulfamoyl, N-(2-dodecyloxyethyl)sulfamoyl,N-ethyl-N-dodecylsulfamoyl, and N,N-diethylsulfamoyl), a sulfonyl group(e.g., an alkyl- or aryl-sulfonyl group having 1 to 36 carbon atoms, forexample, methanesulfonyl, octanesulfonyl, benzenesulfonyl, andtoluenesulfonyl), an alkoxycarbonyl group (e.g., an alkoxycarbonyl grouphaving 2 to 36 carbon atoms, for example, methoxycarbonyl,butyloxycarbonyl, dodecyloxycarbonyl, and octadecyloxycarbonyl), aheterocyclic oxy group (e.g., a heterocyclic oxy group having 1 to 36carbon atoms, for example, 1-phenyltetrazole-5-oxy and2-tetrahydropyranyloxy), an azo group (e.g., phenylazo,4-methoxyphenylazo, 4-pivaroylaminophenylazo, and2-hydroxy-4-propanoylphenylazo), an acyloxy group (e.g., an acyloxygroup having 2 to 36 carbon atoms, for example, acetoxy), a carbamoyloxygroup (e.g., a carbamoyloxy group having 1 to 36 carbon atoms, forexample, N-methylcarbamoyloxy and N-phenylcarbamoyloxy), a silyloxygroup (e.g., silyloxy group having 3 to 36 carbon atoms, for example,trimethylsilyloxy and dibutylmethylsilyloxy), an aryloxycarbonylaminogroup (e.g., an aryloxycarbonyl amino group having 7 to 36 carbon atoms,for example, phenoxycarbonylamino), an imido group (e.g., an imido grouphaving 4 to 36 carbon atoms, for example, N-succinimido, N-phthalimido,and 3-octadecenylsuccinimido), a heterocyclic thio group (e.g., aheterocyclic thio group having 1 to 36 carbon atoms, for example,2-benzothiazolylthio, 2,4-di-phenoxy-1,3,5-tirazole-6-thio, and2-pyridylthio), a sulfinyl group (e.g., a sulfinyl group having 1 to 36carbon atoms, for example, dodecanesulfinyl, 3-pentadecylphenylsulfinyl,and 3-phenoxypropylsulfinyl), an alkyl-, aryl-, or heterocyclic-oxycarbonyl group (e.g., methoxycarbonyl, butoxycarbonyl,dodecyloxycarbonyl, octadecyloxycarbonyl, phenyloxycarbonyl, and2-pentadecyloxycarbonyl), an alkyl-, aryl- or heterocyclic-oxycarbonylamino group (e.g., methoxycarbonylamino,tetradecyloxycarbonylamino, phenoxycarbonylamino, and2,4-di-tert-butylphenoxycarbonylamino), a sulfonamido group (e.g.,methanesulfonamido, hexadecanesulfonamido, benzenesulfonamido,p-toluenesulfonamido, octadecanesulfonamido, and2-methoxy-5-t-butylbenzenesulfonamido), a carbamoyl group (e.g.,N-ethylcarbamoyl, N,N-dibutylcarbamoyl, N-(2-dodecyloxyethyl)carbamoyl,N-methyl-N-dodecylcarbamoyl, andN-{3-(2,4-di-t-amylphenoxy)propyl}carbamoyl), a sulfamoyl group (e.g.,N-ethylsulfamoyl, N,N-dipropylsulfamoyl, N-(2-dodecyloxyethyl)sulfamoyl,N-ethyl-N-dodecylsulfamoyl, and N,N-diethylsulfamoyl), a phosphonylgroup (e.g., phenoxyphosphonyl, octyloxyphosphonyl, andphenylphosphonyl), a sulfamido group (e.g. dipropylsulfamoylamino), animido group (e.g., N-succinimido, hydantoinyl, N-phthalimido, and3-octadecenylsuccinimido), an azolyl group (e.g., imidazolyl, pyrazolyl,3-chloro-pyrazol-1-yl, and triazolyl), a hydroxyl group, a cyano group,a carboxyl group, a nitro group, a sulfo group, an unsubstituted aminogroup.

As R⁶, preferably can be mentioned an alkyl group, an aryl group, aheterocyclic group, a cyano group, a nitro group, an acylamino group, anarylamino group, a ureido group, a sulfamoylamino group, an alkylthiogroup, an arylthio group, an alkoxycarbonylamino group, a sulfonamidogroup, a carbamoyl group, a sulfamoyl group, a sulfonyl group, analkoxycarbonyl group, an aryloxycarbonyl group, a heterocyclic oxygroup, an acyloxy group, a carbamoyloxy group, an aryloxycarbonylaminogroup, an imido group, a heterocyclic thio group, a sulfinyl group, aphosphonyl group, an acyl group, and an azolyl group.

Further preferably an alkyl group or an aryl group, and more preferablyan aryl group whose at least p-position is substituted by an alkylgroup, are mentioned.

X²⁰ represents a heterocyclic ring, a substituted amino group, or anaryl group. As the heterocyclic ring, a 5- to 8-membered ring having anitrogen atom(s), an oxygen atom(s), and/or a sulfur atom(s) and 1 to 36carbon atoms is preferable. A 5- or 6-membered ring bonded through anitrogen atom is more preferable, with particular preference given to a6-membered ring.

As specific examples, imidazole, pyrazole, triazole, lactam compounds,piperidine, pyrrolidine, pyrrole, morpholine, pyrazolidine,thiazolidine, pyrazoline, and the like can be mentioned, with preferencegiven to morpholine and piperidine.

As the substituent of the substituted amino group, an aliphatic group,an aryl group, or a heterocyclic group can be mentioned. As thealiphatic group, the substituents represented by R⁶ as mentioned abovecan be mentioned, which may further be substituted by a cyano group, analkoxy group (e.g., methoxy), an alkoxycarbonyl group (e.g.,ethoxycarbonyl), a chlorine atom, a hydroxyl group, a carboxyl group. Asthe substituted amino group, a di-substituted amino group is morepreferred than a mono-substituted amino group. As the aryl group, onehaving 6 to 36 carbon atoms is preferable, and a single ring is morepreferable. As specific examples, phenyl, 4-t-butylphenyl,2-methylphenyl, 2,4,6-trimethylphenyl, 2-methoxyphenyl, 4-methoxyphenyl,2,6-dichlorophenyl, 2-chlorophenyl, 2,4-dichlorophenyl, and the like canbe mentioned.

Preferable examples of X²⁰ in the case where X²⁰ is a substituted aminogroup are shown below.

Y is a hydrogen atom, or a group capable of being split-off in a processof color development. Examples of the group represented by Y include agroup which can be split-off under an alkaline condition, as describedin, for example, JP-A-61-228444, or a group which can be split-off by acoupling reaction with a developing agent, as described inJP-A-56-133734. Y is preferably a hydrogen atom.

The coupler represented by formula (PTA-III) may be a dimer or morepolymeric compound wherein R⁶ contains a residual group formed from thecoupler represented by formula (PTA-III), or may be a homopolymer orcopolymer wherein R⁶ contains a macromolecular chain. Typical examplesof the homopolymer or copolymer containing a macromolecular chain arehomo- or co-polymers of addition polymerization ethylene-typeunsaturated compounds having a residual group formed from the couplerrepresented by formula (PTA-III). One or more kinds of the cyandye-forming repeating unit having a residual group formed from thecoupler represented by formula (PTA-III) may be contained in thesepolymers. Further, the copolymer may contain as a copolymer ingredient,one or more kinds of a repeating unit derived from a non-coloringethylene-type monomer which does not couple with an oxidation product ofan aromatic primary amine developing agent, such as acrylic acid esters,methacrylic acid esters, and maleic acid esters. The amount of thecompound represented by formula (PTA-III) is preferably 0.01 to 1.0mole, more preferably 0.12 to 1.0 mole, and particularly preferably 0.25to 0.5 mole, per mole of the photosensitive silver halide in the samelayer.

Specific examples of the cyan coupler for use in the present invention,preferably in the fourth embodiment, are shown below. However, thepresent invention is not limited to these compounds.

The compound represented by formula (PTA-III) for use in the presentinvention, preferably in the fourth embodiment, can be synthesized bythe known method, for example, by methods described in JP-A-5-255333,JP-A-5-202004, JP-A-7-48376, and JP-A-8-110623.

Also, as the cyan coupler, a compound represented by formula (IA) shownbelow is preferably used.

In the formula, R′ and R″ each independently represent a substituent,and Z represents a hydrogen atom, or a group capable of being split-offin a coupling reaction with an oxidized product of an aromatic primaryamine color-developing agent.

Note that R′ and R″ are preferably those substituents that are selectedto make the coupler have a preferable hue mentioned in thisspecification.

The term “alkyl” as used herein throughout the present specification,unless otherwise indicated specifically, refers to an unsaturated orsaturated, straight-chain or branched-chain alkyl group (includingalkenyl and aralkyl), including a cyclic alkyl group having 3 to 8carbon atoms (including cycloalkenyl), and the term “aryl” specificallyincludes a condensed aryl.

With respect to formula (IA), R′ and R″ are preferably selectedindependently from an unsubstituted or substituted alkyl group, arylgroup, amino group or alkoxy group, or 5- to 10-membered heterocyclecontaining at least one heteroatom selected from nitrogen, oxygen andsulfur (the ring being unsubstituted or substituted).

When R′ and/or R″ are an amino group or an alkoxy group, they may besubstituted with, for example, a halogen atom, an aryloxy group, or analkyl- or aryl-sulfonyl group. Preferably, R′ and R″ are independentlyselected from unsubstituted or substituted, alkyl or aryl groups, orfive to ten-membered heterocyclic groups, such as a pyridyl group, amorpholino group, an imidazolyl group, and a pyridazolyl group.

R′ is preferably an alkyl group substituted with, for example, a halogenatom, an alkyl group, an aryloxy group, or an alkyl- or aryl-sulfonylgroup (which may be further substituted). When R″ is an alkyl group, itmay also be substituted in the same manner as described above.

However, R′ is preferably an unsubstituted aryl group, or a heterocyclicgroup substituted with, for example, a cyano group, a chlorine atom, afluorine atom, a bromine atom, an iodine atom, an alkyl- oraryl-carbonyl group, an alkyl- or aryl-oxycarbonyl group, an acyloxygroup, a carbonamido group, an alkyl- or aryl-carbonamido group, analkyl- or aryl-oxycarbonamido group, an alkyl- or aryl-sulfonyl group,an alkyl- or aryl-sulfonyloxy group, an alkyl- or aryl-oxysulfonylgroup, an alkyl- or aryl-sulfoxide group, an alkyl- or aryl-sulfamoylgroup, an alkyl- or aryl-sulfamoylamino group, an alkyl- oraryl-sulfonamido group, an aryl group, an alkyl group, an alkoxy group,an aryloxy group, a nitro group, an alkyl- or aryl-ureido group, or analkyl- or aryl-carbamoyl group (each of which may by furthersubstituted). Preferred substituent groups are a halogen atom, a cyanogroup, an alkoxycarbonyl group, an alkylsulfamoyl group, analkyl-sulfonamido group, an alkylsulfonyl group, a carbamoyl group, analkylcarbamoyl group, and an alkylcarbonamido group. When R′ is an arylgroup or a heterocyclic group, it may also be substituted in the samemanner as described above.

Preferably, R″ is a 4-chlorophenyl group, a 3,4-dichlorophenyl group, a3,4-difluorophenyl group, a 4-cyanophenyl group, 3-chloro-4-cyano-phenylgroup, a pentafluorophenyl group, or a 3- or 4-sulfonamido-phenyl group.

In formula (IA), Z represents a hydrogen atom or a group that can splitoff upon a coupling reaction with an oxidized product of an aromaticprimary amine color-developing agent. Z is preferably a hydrogen atom, achlorine atom, a fluorine atom, a substituted aryloxy or amercaptotetrazole, more preferably a hydrogen atom or a chlorine atom.

Z determines the chemical equivalent of the coupler, that is, whether itis a two-equivalent coupler or a four-equivalent coupler, and thereactivity of the coupler can be changed depending on the kind of Z.Such a group can give advantageous effects on the layers on which thecoupler is coated or other layers in a photographic recording material,by exhibiting a function, for example, of dye formation, dye hueadjustment, acceleration of development or inhibition of development,acceleration of bleaching or inhibition of bleaching, facilitation ofelectron mobilization, color correction, or the like, after it isreleased from the coupler.

Examples of representative class of such a coupling split-off groupinclude halogen, alkoxy, aryloxy, heterocyclyloxy, sulfonyloxy, acyloxy,acyl, heterocyclyl, sulfonamido, heterocylylthio, benzothiazolyl,phosphonyloxy, alkylthio, arylthio, and arylazo groups. These couplingsplit-off groups are described, for example, in the followingspecifications: U.S. Pat. No. 2,455,169, U.S. Pat. No. 3,227,551, U.S.Pat. No. 3,432,521, U.S. Pat. No. 3,467,563, U.S. Pat. No. 3,617,291,U.S. Pat. No. 3,880,661, U.S. Pat. No. 4,052,212, and U.S. Pat. No.4,134,766, as well as GB Patent No. 1,466,728, GB Patent No. 1,531,927,and GB Patent No. 1,533,039, and GB Patent application publication Nos.2,066,755 and 2,017,704, the disclosure of which are incorporated hereinby reference. Most preferred are a halogen atom, an alkoxy group, and anaryloxy group.

Preferable examples of the coupling split-off group are as follows: —Cl,—F, —Br, —SCN, —OCH₃, —OC₆H₅, —OCH₂C(═O)NHCH₂CH₂OH,—OCH₂C(O)NHCH₂CH₂OCH₃, —OCH₂C(O)NHCH₂CH₂OC(═O)OCH₃, —P(O) (OC₂H₅)₂,—SCH₂CH₂COOH,

In general, the coupling split-off group is a chlorine atom, a hydrogenatom, or a p-methoxyphenoxy group.

Specific examples of the compound represented by formula (IA) are shownbelow. However, the present invention is not limited to these compounds.

The content of the cyan dye-forming coupler represented by the formula(IA) that is preferably used in the present invention, preferably in thefourth embodiment, in the photosensitive material, is generally 0.01g/m² to 10 g/m², preferably 0.1 g/m² to 2 g/m², and it is generally1×10⁻³ mole to 1 mole, preferably 2×10⁻³ mole to 3×10⁻¹ mole, per moleof the silver halide in the same photosensitive emulsion layer.

In the present invention, preferably in the fourth embodiment, asurface-active agent may be added to the light-sensitive material, inview of improvement in coating-stability, prevention of staticelectricity from generation, and adjustment of charge amount. As thesurface-active agent, there are anionic, cationic, betaine and nonionicsurfactants. Examples thereof include those described in JP-A-5-333492.As the surface-active agent for use in the present invention, preferablyin the fourth embodiment, a fluorine-containing surface-active agent ispreferred. In particular, fluorine-containing surface-active agents asshown below can be preferably used. These fluorine-containingsurface-active agents may be used singly, or may be used in combinationwith another known surfactant. Preferably, the fluorine-containingsurfactant is used in combination with another known surfactant. Theamount of these surface-active agents to be added to the light-sensitivematerial is not particularly limited, but it is generally in the rangeof 1×10⁻⁵ to 1 g/m², preferably in the range of 1×10⁻⁴ to 1×10⁻¹ g/m²,more preferably in the range of 1×10⁻³ to 1×10⁻² g/m².

In the present invention, preferably in the fourth embodiment, as astill more preferable example, a fluorine-containing surfactant of theformula (1) shown below may be mentioned.

In the formula (1), A and B each independently represent a fluorine atomor a hydrogen atom. a and b each independently are an integer of 1 to 6.c and d each independently are an integer of 4 to 8. x is 0 or 1. Mrepresents a cation.

It is preferred that both A and B are fluorine atoms or hydrogen atoms,and that more preferably both A and B are fluorine atoms.

a and b are preferably an integer of 1 to 6 with a=b, more preferably 2or 3 with a=b, and further more preferably a=b=2.

c and d are preferably an integer of 4 to 6 with c=d, more preferably 4or 6 with c=d, and further more preferably c=d=4.

x is 0 or 1 and both cases are equally preferable.

As the cation represented by M, an alkali metal ion (for example,lithium ion, sodium ion, potassium ion, etc.), an alkaline earth metalion (for example, barium ion, calcium ion, etc.), an ammonium ion, etc.are preferably used. Among those, particularly preferred are lithiumion, sodium ion, potassium ion, and ammonium ion.

The compound represented by the formula (1) is more preferably acompound represented by the formula (1-a) shown below.

In the formula (1-a), a, b, c, d, M, and x each have the same meaningsas those in the formula (1) and the same is true for the preferredranges.

The compound represented by the formula (1) is further more preferably acompound represented by the formula (1-b) shown below.

In the formula (1-b), a¹ is an integer of 2 or 3. c¹ is an integer of 4to 6. M represents a cation.

a¹ is preferably 2, and c¹ is preferably 4.

x is 0 or 1, and both cases are equally preferred.

Hereinafter, specific examples of the compound (surfactant) representedby formula (1) are shown below. However, the compound for use in thepresent invention is not limited thereto.

The compounds (surfactants) represented by the formula (1), (1-a) or(1-b) described above preferably used in the present invention, morepreferably in the fourth embodiment, can be readily synthesized by acombination of the general esterification reaction and sulfonationreaction. The conversion of the counter cation can be readily performedby use of an ion exchange resin.

Hereinafter, representative examples of the synthesis method will bedescribed. However, the present invention should not be considered asbeing limited to these specific synthetic examples.

Synthetic Example 4-1 Synthesis of Exemplified Compound FS-1 1-1Synthesis of di(3,3,4,4,5,5,6,6,6-nonafluorohexyl) maleate

9.8 g (0.10 mol) of maleic anhydride, 52.8 g (0.20 mol) of3,3,4,4,5,5,6,6,6-nonafluorohexanol, and 0.5 g of p-toluenesulfonic acidmonohydrate in 30 milliliters (hereinafter, also referred to as “mL”) oftoluene, were heated under reflux for 24 hours while distilling offwater produced. Thereafter, the reaction mixture was cooled to roomtemperature and hexane and ethyl acetate were added thereto. The organicphase was washed with 1 mol/litter (hereinafter, also referred to as“L”) of an aqueous sodium hydroxide solution and an aqueous saturatedsodium chloride solution, dried over sodium sulfate, and then afterremoving the solvent under reduced pressure, purified by silica gelcolumn chromatography (hexane/ethyl acetate: 9/1 to 8/2 v/v) to obtain53.2 g (yield 88%) of the objective compound as a white solid.

1-2 Synthesis of FS-1

42.8 g (69 mmol) of di(3,3,4,4,5,5,6,6,6-nonafluorohexyl) maleate, and7.9 g (76 mmol) of sodium hydrogen sulfite, and 50 mL of water-ethanol(1/1 v/v) were added and heated under reflux for 3 hours. Then, theresultant was cooled to 0° C. and the solid precipitated was collected,followed by recrystallization operation from acetonitrile. The crystalobtained was dried under reduced pressure at 60° C. to obtain 27.0 g(yield 54%) of the objective compound as a white crystal.

¹H-NMR data of the obtained compound is shown below. ¹H-NMR (DMSO-d₆) δ2.49-2.62 (m, 4H), 2.85-2.99 (m, 2H), 3.68 (dd, 1H), 4.23-4.35 (m, 4H)

Synthetic Example 4-2 Synthesis of Exemplified Compound PS-2 2-1Synthesis of di(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl) maleate

4.61 g (47 mmol) of maleic anhydride, 34.1 g (98 mmol) of3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylalcohol, and 0.24 g ofp-toluenesulfonic acid monohydrate in 140 mL of toluene, were heatedunder reflux for 10 hours while distilling off water produced.Thereafter, the reaction mixture was cooled to room temperature andethyl acetate were added thereto. The organic phase was washed with anaqueous saturated sodium chloride solution, dried over sodium sulfate,and then after removing the solvent under reduced pressure, purified bysilica gel column chromatography (hexane/ethyl acetate: 8/2 v/v) toobtain 19.7 g (yield 52%) of the objective compound as a white solid.

2-2 Synthesis of FS-2

10.0 g (12.4 mmol) of di(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)maleate, and 1.55 g (14.9 mmol) of sodium hydrogen sulfite, and 15 mL ofwater-ethanol (1/1 v/v) were added and heated under reflux for 7 hours.Then, the resultant was cooled to room temperature. The crystal obtainedwas dried under reduced pressure at 60° C. to obtain 9.38 g (yield 81%)of the objective compound as a white crystal.

¹H-NMR data of the obtained compound is shown below. ¹H-NMR (DMSO-d₆) δ2.48 (m, 4H), 2.97 (m, 2H), 3.82 (m, 1H), 4.18-4.58 (m, 4H)

Synthetic Example 4-3 Synthesis of Exemplified Compound FS-4 3-1Synthesis of di(4,4,5,5,6,6,7,7,7-nonafluoroheptyl) maleate

17.6 g (0.18 mol) of maleic anhydride, 100 g (0.36 mol) of4,4,5,5,6,6,7,7,7-nonafluoroheptanol, and 0.5 g of p-toluenesulfonicacid monohydrate in 250 mL of toluene, were heated under reflux for 12hours while distilling off water produced. Thereafter, the reactionmixture was cooled to room temperature and chloroform was added thereto.The organic phase was washed with 1 mol/L of an aqueous sodium hydroxidesolution and an aqueous saturated sodium chloride solution, to obtain114.1 g of the objective compound as a white solid quantitatively.

3-2 Synthesis of FS-4

95.8 g (156 mmol) of di(4,4,5,5,6,6,7,7,7-nonafluoroheptyl) maleate, 7.9g (172 mmol) of sodium hydrogen sulfite, and 100 mL of water-ethanol(1/1 v/v) were added and heated under reflux for 20 hours. Then, ethylacetate was added thereto and the organic phase was washed with anaqueous saturated sodium chloride solution and dried over sodiumsulfate. Thereafter, the solvent was concentrated under reducedpressure, followed by performing recrystallization operation fromacetonitrile. The crystal obtained was dried under reduced pressure at60° C. to obtain 95.8 g (yield 83%) of the objective compound as a whitecrystal.

¹H-NMR data of the obtained compound is shown below. ¹H-NMR (DMSO-d₆) δ1.80 (m, 4H), 2.19-2.34 (m, 4H), 2.79-2.97 (m, 2H), 3.68 (dd, 1H),4.01-4.29 (m, 4H)

Synthetic Example 4-4 Synthesis of FS-19 4-1 Synthesis ofdi(3,3,4,4,5,5,6,6,6-nonafluorohexyl) itaconate

13.5 g (0.12 mol) of itaconic anhydride, 69.8 g (0.26 mol) of3,3,4,4,5,5,6,6,6-nonafluorohexanol, and 1.14 g (6 mmol) ofp-toluenesulfonic acid monohydrate in 500 mL of toluene, were heatedunder reflux for 12 hours while distilling off water produced.Thereafter, the reaction mixture was cooled to room temperature andethyl acetate was added thereto. The organic phase was washed with 1mol/L of an aqueous sodium hydroxide solution and an aqueous saturatedsodium chloride solution to obtain 51.3 g (yield 69%) of the objectivecompound as an oily compound.

4-2 Synthesis of FS-19

20.0 g (32 mmol) of di(3,3,4,4,5,5,6,6,6-nonafluorohexyl) itaconate, and4.0 g (38 mmol) of sodium hydrogen sulfite, and 25 mL of water-ethanol(1/1 v/v) were added and heated under reflux for 6 hours. Then, ethylacetate was added thereto and the organic phase was washed with anaqueous saturated sodium chloride solution and dried over sodiumsulfate. Thereafter, the solvent was concentrated under reducedpressure, followed by performing recrystallization operation fromacetonitrile. The crystal obtained was dried under reduced pressure at80° C. for 2 hours to obtain 20.6 g (yield 89%) of the objectivecompound as a white crystal.

¹H-NMR data of the obtained compound is shown below. ¹H-NMR (DMSO-d₆) δ2.49-2.78 (m, 5H), 3.04-3.13 (m, 2H), 3.47 (br, 2H), 4.23 (t, 4H)

In the present invention, preferably in the fourth embodiment, in thecase where the above-mentioned surfactant is used in the layers of aphotographic light-sensitive material, the aqueous coating compositioncontaining the surfactant may consist of the surfactant used preferablyin the present invention, preferably in the fourth embodiment, andwater, or may contain another component as needed depending on thepurpose.

In the above-mentioned aqueous coating composition, the surfactant usedin the present invention, preferably in the fourth embodiment, may beused singly, or as a mixture of two or more thereof. Moreover, asurfactant other than the surfactant for use in the present inventionmay be used in combination with the surfactant for use in the presentinvention. The surfactant which can be combined with the surfactant foruse in the present invention includes various surfactants such asanionic-, cationic-, and nonionic surfactants. Those surfactants may bea polymeric surfactant, or may be a fluorine-containing surfactant thatis one other than the surfactant used in the present invention,preferably in the fourth embodiment. Among those, an anionic- ornonionic surfactant is more preferred. Examples of the surfactant whichcan be combined with the surfactant used in the present invention,include those described in, for example, JP-A-62-215272 (pp. 649-706),and Research Disclosure (RD) Item 17643, pp. 26-27 (December, 1978), RDItem 18716, p. 650 (November, 1979), and RD Item 307105, pp. 875-876(November, 1989).

A representative example of materials which may be contained in theabove-mentioned aqueous coating composition is a polymeric compound. Thepolymeric compound may be an aqueous medium-soluble polymer, or may be apolymer dispersion in water (that is, a polymeric latex). The solublepolymer is not particularly limited, and includes, for example, gelatin,a polyvinyl alcohol, casein, agar, acacia gum, hydroxyethylcellulose,methylcellulose, and carboxymethylcellolose. The polymeric latexincludes dispersions of: homo- or copolymers of various vinyl monomers(for example, acrylate derivatives, methacrylate derivatives, acrylamidederivatives, methacrylamide derivatives, styrene derivatives, conjugatediene derivatives, N-vinyl compounds, O-vinyl compounds, vinyl nitrile,and other vinyl compounds (such as ethylene, and vinylidene chloride));or condensation-series polymers (for example, polyesters, polyurethanes,polycarbonates, polyamides). Detailed examples for such polymericcompounds can include, for example, those described in JP-A-62-215272(pp. 707-763), and Research Disclosure (RD) Item 17643, p. 651(December, 1978), RD Item 18716, p. 650 (November, 1979), and RD Item307105, pp. 873-874 (November, 1989).

The medium for the above-mentioned aqueous coating composition may bewater alone, or a mixed solvent of an organic solvent (for example,methanol, ethanol, isopropyl alcohol, n-butanol, methyl cellosolve,dimethylformamide, acetone, etc.) and water. The proportion of water inthe medium for the aqueous coating composition is preferably 50% ormore.

The above-mentioned aqueous coating composition may contain variouscompounds depending on the layer of the photographic light-sensitivematerial to be used. Such compounds may be dissolved or dispersed in amedium. Examples thereof include various couplers, ultravioletabsorbents, anti-color mixing agents, antistatic agents, scavengers,antifog agents, hardening agents, dyes, fungicides, and the like. Toobtain effective antistatic ability and uniformity of coating when usedin a photographic light-sensitive material, they are used preferably inthe uppermost hydrophilic colloid layer.

In this case, the coating composition in the uppermost hydrophiliccolloid layer may contain besides hydrophilic colloid (for example,gelatin) and the fluorine-series surfactant used in the presentinvention, preferably in the fourth embodiment, other surfactants,matting agents, lubricants, colloidal silica, gelatin plasticizers, andthe like.

The use amount of the compounds (surfactants) represented by the formula(I), (1-a) or (1-b) is not particularly limited and the use amount maybe varied optionally depending on the structure and application of thesurfactant, the kind and amount of compounds contained in the aqueouscomposition, the constitution of the medium, and the like. For example,in the case where the surfactant used in the present invention,preferably in the fourth embodiment, is used in a coating solution forthe uppermost hydrophilic colloid (gelatin) layer in the photographiclight-sensitive material that is one preferred embodiment of the presentinvention, the use amount of the surfactant in terms of theconcentration (mass %) in the coating solution is preferably 0.003 to0.5%, and preferably 0.03 to 5% based on the gelatin solid content.

Further, the above water-resistant resin layers on the reflective-typebase preferably contain a fluorescent whitening agent. Further, afluorescent whitening agent may be dispersed in the hydrophilic colloidlayer of the light-sensitive material. As the fluorescent whiteningagent, preferably a benzoxazole-series fluorescent whitening agent, acoumarin-series fluorescent whitening agent, or apyrazoline-series-fluorescent whitening agent can be used, and morepreferably a benzoxazolylnaphthalene-series fluorescent whitening agentor a benzoxazolylstilbene-series fluorescent whitening agent is used.Specific examples of the fluorescent whitening agent that is containedin a water-resistant resin layer, include, for example,4,4′-bis(benzoxazolyl)stilbene, 4,4′-bis(5-methylbenzoxazolyl)stilbene,and mixture of these. The amount to be used is not particularly limited,but preferably it is 1 to 100 mg/m². When it is mixed with awater-resistant resin, preferably the mixing proportion is 0.0005 to 3%by weight, and more preferably 0.001 to 0.5% by weight, to the resin.

The reflective-type base may be one wherein a hydrophilic colloid layercontaining a white pigment is applied on a transmission-type base, or areflective-type base described in the above.

Further, the reflective-type base may be a base having a specularreflective- or a second-type diffusion reflective metal surface.

A more preferable reflective support for use in the present invention,preferably in the fourth embodiment, is a support having a papersubstrate provided with a polyolefin layer having fine holes, on thesame side as silver halide emulsion layers. The polyolefin layer may becomposed of multi-layers. In this case, it is more preferable for thesupport to be composed of a fine hole-free polyolefin (e.g.,polypropylene, polyethylene) layer adjacent to a gelatin layer on thesame side as the silver halide emulsion layers, and a finehole-containing polyolefin (e.g., polypropylene, polyethylene) layercloser to the paper substrate. The density of the multi-layer orsingle-layer of polyolefin layer(s) existing between the paper substrateand photographic constituting layers is preferably in the range of 0.40to 1.0 g/ml, more preferably in the range of 0.50 to 0.70 g/ml. Further,the thickness of the multi-layer or single-layer of polyolefin layer(s)existing between the paper substrate and photographic constitutinglayers is preferably in the range of 10 to 100 μm, more preferably inthe range of 15 to 70 μm. Further, the ratio of thickness of thepolyolefin layer(s) to the paper substrate is preferably in the range of0.05 to 0.2, more preferably in the range 0.1 to 0.15.

Further, it is also preferable for enhancing rigidity (mechanicalstrength) of the reflective support, by providing a polyolefin layer onthe surface of the foregoing paper substrate opposite to the side of thephotographic constituting layers, i.e., on the back surface of the papersubstrate. In this case, it is preferable that the polyolefin layer onthe back surface be polyethylene or polypropylene, the surface of whichis matted, with the polypropylene being more preferable. The thicknessof the polyolefin layer on the back surface is preferably in the rangeof 5 to 50 μm, more preferably in the range of 10 to 30 μm, and furtherthe density thereof is preferably in the range of 0.7 to 1.1 g/ml. As tothe reflective support for use in the present invention, preferably inthe fourth embodiment, preferable embodiments of the polyolefin layerprovide on the paper substrate include those described inJP-A-10-333277, JP-A-10-333278, JP-A-11-52513, JP-A-11-65024, EuropeanPatent Nos. 0880065 and 0880066.

It is preferred that the silver halide color photographiclight-sensitive material of the present invention, preferably of thefourth embodiment, is imagewise exposed to coherent light from a bluelaser having an emission-wavelength of 420 nm to 460 nm. Among the bluelasers, it is particularly preferable to use a blue semiconductor laser.

Examples of the semiconductor laser include blue semiconductor laserhaving a wavelength of 430 to 450 nm (Presentation by Nichia Corporationat the 48^(th) Applied Physics Related Joint Meeting, in March, 2001), ablue laser at about 470 nm obtained by wavelength modulation of asemiconductor laser (oscillation wavelength about 940 nm) with a SHGcrystal of LiNbO₃ having a reversed domain structure in the form of awave guide, a green laser at about 530 nm obtained by wavelengthmodulation of a semiconductor laser (oscillation wavelength about 1,060nm) with a SHG crystal of LiNbO₃ having a reversed domain structure inthe form of a wave guide, a red semiconductor laser having a wavelengthof about 685 nm (Type No. HL6738MG (trade name), manufactured byHitachi, Ltd.), a red semiconductor laser having a wavelength of about650 nm (Type No. HL6501MG (trade name), manufactured by Hitachi, Ltd.),and the like.

Exposure to light may be performed in plural times to the samephotosensitive layer. In this case, it is preferred that the exposure isperformed at least three times. Particularly preferably, an exposuretime is 10⁻³ second or more (preferably 10⁻⁴ to 10⁻⁸ second). In thecase where the exposure time is 10⁻⁵ to 10⁻⁸ second, it is preferredthat the exposure be performed at least eight times. As a light source,any light source may be used. For example, a gas laser, a solid laser(LD), LED (organic or inorganic), a Xe light source with a restrictedspot. In particular, a solid laser and LED are preferred. The lightsource must be spectrally separated to color-sensitive wavelength ofeach dye-forming layer. For this purpose, a suitable color filter (whichcontains or is deposited with a dye) is used or the oscillationwavelength of LD or LED may be selected. Further, both of these may beused in combination. The spot diameter of the light source is notparticularly limited and is preferably 5 to 250 μm, and particularlypreferably 10 to 100 μm, in terms of a half width value of lightintensity. The shape of the spot may be any of a circle, an ellipse, ora rectangle. The distribution of the quantity of light of one spot maybe of a Gaussian distribution or a trapezoid with a relatively constantlight intensity. In particular, the light source may either consist ofone or an array of plural light sources.

In the present invention, preferably in the fourth embodiment,generally, exposure to light is performed by scanning exposure. Thelight source may be scanned, or the photosensitive material may bescanned. Also, both may be scanned. The exposure time for a single runis defined by the following equation.Exposure time=Spot diameter/Moving speed of light source (or Movingspeed of photosensitive material)

Here, the spot diameter refers to the diameter of a spot (half widthvalue, unit: μm) in the direction in which the light source used inscanning exposure moves at the time of exposure. Further, the movingspeed of light source refers to the speed (unit: μm/second) at which thelight source used for scanning exposure moves per unit time. Generally,the spot diameter does not have to be the same as the diameter of thepixel, and may be either greater or smaller than that. The number oftimes of exposure as used herein refers to the number of times ofirradiation of light is sensed by the same color-sensitive layer at asingle point (pixel) of the photosensitive material. In the case whereirradiation is performed in plural times, it refers to the number oftimes of exposure performed at an intensity ⅕ time or more of themaximum intensity of light to which the material is exposed. Therefore,exposure performed at an intensity below ⅕ time of the maximum intensityof light, stray light, or overlap between the spots, are not countedinto the number of times.

The silver halide color photographic light-sensitive material of thepresent invention is excellent in color reproducibility. The silverhalide color photographic light-sensitive material of the presentinvention is excellent in rapid processing suitability.

The silver halide color photographic light-sensitive material of thepresent invention is excellent in rapid processing suitability. Further,the silver halide color photographic light-sensitive material of thepresent invention is excellent in color reproducibility, storagestability in unexposed state of the light-sensitive material, and imagefastness after processing.

According to the present invention, can be provided a silver halidecolor photographic light-sensitive material that is excellent in rapidhigh-productivity processing suitability and achieves remarkable costreduction; and a method of forming an image by using the abovelight-sensitive material can also be provided. Further, according to thepresent invention, can be provided a silver halide color photographiclight-sensitive material with a layer structure designed, taking intoconsideration the balance among the coupling rates of the couplers to beused, to increase the reaction efficiency of the oxidized developingagent generated at the time of color development, to reduce the coatingamount of materials, and to enable shortening of the image-forming time,bleach-fixing time, and rinsing time without any trouble in colordevelopment; and a method of forming an image by using the abovelight-sensitive material can also be provided.

The silver halide color photographic light-sensitive material of thepresent invention is excellent in a property for preventingstatic-induced fog. According to the present invention, the property forpreventing static-induced fog of the light-sensitive material can beimproved, while maintaining good sharpness of an image formed and highprocessing suitability of the light-sensitive material withoutdeteriorating these properties.

The silver halide color photographic light-sensitive material of thepresent invention is excellent in color reproducibility. Further, thesilver halide color photographic light-sensitive material of the presentinvention is excellent in rapid processing suitability, in addition tocolor reproducibility.

The silver halide color photographic light-sensitive material of thepresent invention is excellent in rapid processing suitability. Further,the silver halide color photographic light-sensitive material of thepresent invention is also excellent in color reproducibility, storagestability thereof in an unexposed state, and image fastness afterprocessing, in addition to rapid processing suitability.

The silver halide color photographic light-sensitive material of thepresent invention exhibits such excellent effects as capable ofincreasing the reaction efficiency of the oxidized developing agentgenerated at the time of color development, reducing the coating amountof materials, and enabling shortening of the image-forming time,bleach-fixing time, and rinsing time without any troubles in colordevelopment.

Hereinafter, the present invention will be described in more detailbased on examples given below, but the present invention is not meant tobe limited thereto.

EXAMPLE

Numbering system of the compounds and simplified symbols, and the like,as utilized in each of the examples are independent in each of theexamples, unless otherwise specified.

Example 1-1 Support

A support used in the present example was prepared with the below shownmethod.

1) First Layer and Undercoat Layer

The two surfaces of the 90 μm thick polyethylenenaphthlate supports weresubjected to glow discharge treatment under the conditions of processingatmospheric pressure: 2.66×10 Pa; H₂O partial pressure in theatmospheric vapor: 75%; discharge frequency: 30 kHz; output: 2500 W; andprocessing intensity: 0.5 kV A minute/m². After that, one surface of thesupport was coated with a coating solution having the followingcomposition for the first layer so as to give a coating amount of 5ml/m², by a bar coat method described in JP-B-58-4589.

A dispersion liquid of conductive fine particles (10% aqueous dispersionof SnO₂/Sb₂O₅ particles. Secondary aggregate, whose average particlediameter 50 mass parts was 0.05 μm, composed of particles whose primaryparticle diameter was 0.005 μm.) Gelatin 0.5 mass part Water 49 massparts Polyglycerolpolyglycidyl ether 0.16 mass part Poly(polymerizationdegree 20)oxyethylene 0.1 mass part sorbitan mono-laurate

Further, after coating the first layer, the polyethylenenaphthlate (PEN)support was wound around a stainless steel core of 20 cm in diameter andgiven a thermal history by heating at 110° C. (Tg of PEN support: 119°C.) for 48 hours. Thus, an annealing treatment was completed. The othersurface of the support opposite to the first layer was coated with acoating solution having the following composition as an undercoat layerfor an emulsion, so as to give a coating amount of 10 ml/m², by using abar coat method. Gelatin 1.01 mass parts Salicylic acid 0.30 mass partResorcin 0.40 mass part Poly(polymerization degree 10)oxyethylene 0.11mass part nonylphenylether Water 3.53 mass parts Methanol 84.57 massparts n-Propanol 10.08 mass parts

Further, the second layer and the third layer described later werecoated on the first layer in this order. At last, the color negativelight-sensitive material having the composition described later wasmulti-coated on the opposite side, so that a transparent magneticrecording medium with a silver halide emulsion was prepared.

2) Second Layer (Transparent Magnetic Recording layer)

(i) Dispersion of Magnetic Substance

1100 mass parts of Co-coated γ-Fe₂O₃ magnetic substance (average majoraxis length: 0.25 μm, SBET: 39 m²/g, Hc: 6.56×10⁴ A/m, σ_(s): 77.1 Am²/kg, or: 37.4 A m²/kg), 220 mass parts of water, 165 mass parts ofsilane coupling agent (3-(poly(polymerization degree10)oxyethynyl)oxypropyl trimethoxysilane) were added and well mixed bymeans of an open kneader for 3 hours. The resulting roughly dispersedviscous liquid was dried at 70° C. for a day (one day and one night) toremove water. Thereafter, a heat treatment was performed at 110° C. for1 hour to prepare surface-treated magnetic particles.

Further, a mixture having the following formulation was kneaded again bymeans of an open kneader for 4 hours. The above-mentionedsurface-treated 855 g magnetic particles Diacethylcellulose 25.3 gMethylethylketone 136.3 g Cyclohexanone 136.3 g

Further, a mixture having the following formulation was finely dispersedat 2,000 rpm by means of a sand mill (1/4 G sand mill), for 4 hours. 1mmø-glass beads were used as a media. The above kneaded solution 45 gDiacethylcellulose 23.7 g Methylethylketone 127.7 g Cyclohexanone 127.7g

Further, an intermediate solution containing a magnetic substance wasprepared according to the following formulation.

(ii) Preparation of Intermediate Solution Containing a MagneticSubstance The above-described magnetic substance finely dispersed 674 gsolution Diacethyl cellulose solution 24280 g (Solid content: 4.34%,Solvent: methylethylketone/cyclohexanone = 1/1) Cyclohexanone 46 g

These were mixed and stirred by a dispersing means (Disper) to preparean “intermediate solution containing a magnetic substance”.

A dispersion solution of a-alumina abrasive having the followingformulation for use in the present invention was prepared.

(a) Sumicorundum AA-1.5 (average primary particle diameter of 1.5 μm,specific surface area of 1.3 m²/g, trade name, manufactured by SumitomoChemical Co., Ltd.)

Preparation of Particle Dispersion Solution Sumicorundum AA-1.5 (tradename, manufactured by 152 g Sumitomo Chemical Co., Ltd.) Silane couplingagent KBM 903 (trade name, 0.48 g manufactured by Shinetsu silicone Co.)Diacetyl cellulose solution 227.52 g (solid content 4.5%, solvent:methyl ethylketone/cyclohexanone = 1/1)

The mixture having the above formulation was finely dispersed by meansof a ceramic-coated sand mill (1/4 G), at the rate of 800 rpm, for 4hours. As a media, zirconia beads having a diameter of 1 mmφ were used.

(b) Colloidal Silica Particle-Dispersed Solution (Fine Particles)

“MEK-ST” (trade name) manufactured by Nissan Chemical Industries Ltd.was used.

This was a dispersed solution of colloidal silica having average primaryparticle diameter of 0.015 μm in methyl ethyl ketone as a dispersionmedium, and the solid content of the colloidal silica was 30%.

(iii) Preparation of Second Layer Coating Solution The above-describedmagnetic substance-containing 19053 g intermediate solution Diacetylcellulose solution 264 g (solid content 4.5%, solvent:methylethylketone/ cyclohexanone = 1/1) Colloidal silica dispersionsolution (MEK-ST) 128 g (dispersion solution b) (solid content 30%)Sumicorundum AA-1.5 dispersed solution 12 g (dispersion solution a)Millionate MR-400 (trade name, manufactured by Nippon 203 g PolyurethaneCo., Ltd.) diluted solution (solid content 20%, diluting solvent: methylethylketone/cyclohexanone = 1/1) Methyl ethyl ketone 170 g Cyclohexanone170 g

The coating solution, which was obtained by mixing and stirring theabove, was coated in a coating amount of 29.3 ml/m² by means of a wirebar. Drying of the coated layer was performed at 110° C. The thicknessof the dried magnetic layer was 1.0 μm.

3) Third Layer (a Layer Containing a Higher Fatty Acid Ester Lubricant)

(i) Preparation of Undiluted Dispersion Solution Containing a Lubricant

Solution A presented below was dissolved by heating at 100° C. Theresultant solution was added to Solution B, and then the resultantmixture was dispersed by means of a high pressure homogenizer to preparean undiluted dispersion solution containing a lubricant.

Solution A The compound shown below 399 mass partsC₆H₁₃CH(OH)(CH₂)₁₀COOC₅₀H₁₀₁ The compound shown below 171 mass partsn-C₅₀H₁₀₁O(CH₂CH₂O)₁₆H Cyclohexanone 830 mass parts Solution BCyclohexanone 8600 mass parts (ii) Preparation of Spherical Inorganic Particle Dispersion Solution

Spherical inorganic particle dispersion solution (c1) was preparedaccording to the following formulation. Isopropyl alcohol 93.54 massparts Silane coupling agent KEM 903 (trade name, manufactured byShinetsu silicone Co.) compound 1-1: (CH₃O)₃Si—(CH₂)₃—NH₂  5.53 massparts Compound 1  2.93 mass parts Compound 1

SEA HOSTER KEP 50 88.00 mass parts

-   -   (amorphous spherical silica having an average grain diameter of        0.5 μm; trade name, manufactured by NIPPON SHOKUBAI CO., LTD.)

The mixture having the above-mentioned formulation was stirred for 10minutes. Then, the following was further added. Diacetone alcohol 252.93mass parts

An ultrasonic homogenizer SONIFIER 450 (trade name, manufactured byBRANSON Co., Ltd.) was used to disperse the resultant mixture solutionfor 3 hours with stirring while cooling on ice. Thus, a dispersionsolution cl of spherical inorganic particles was completed.

(iii) Preparation of a Dispersion Solution Containing Spherical OrganicHigh Molecular Particles

A dispersion solution (c2) containing spherical organic high molecularparticles was prepared according to the following formulation.XC99-A8808 (trade name, manufactured by Toshiba  60 mass parts SiliconeCo., Ltd.; spherical cross-linking polysiloxane particles having anaverage grain size of 0.9 μm) Methylethylketone 120 mass partsCyclohexanone 120 mass parts

(Solid content 20%, Solvent: methylethylketone/cyclohexane=1/1)

An ultrasonic homogenizer SONIFIER 450 (trade name, manufactured byBRANSON Co., Ltd.) was used to disperse the resultant mixture solutionfor 2 hours with stirring while cooling on ice. Thus, a dispersionsolution c2 of spherical organic high-molecular particles was completed.

(iv) Preparation of Third Layer Coating Solution

The following compositions were added to 542 g of the aforementionedundiluted dispersion solution containing a lubricant, so that the thirdlayer coating solution was formed. Diacetone alcohol 5950 gCyclohexanone 176 g Ethyl acetate 1700 g The aforementioned dispersionsolution (c1) of SEA 53.1 g HOSTER KEP 50 The aforementioned dispersionsolution (c2) 300 g of spherical organic high molecular particles FC431(trade name, manufactured by 3M Co., Ltd., 2.65 g solid content 50%,Solvent: Ethyl acetate) BYK310 (trade name, manufactured by BYK ChemJapan 5.3 g Co., Ltd, Solid content: 25%)

The above third layer coating solution was coated on the second layer ina coating amount of 10.35 ml/m² followed by drying at 110° C., andfurther dried at 97° C. for 3 minutes.

4) Coating of Photosensitive Layer

Then, the opposite surface of the backing layer obtained above wasmulti-coated with each of the layers of the following composition toprepare a color-negative film.

(Composition of the Photosensitive Layer)

The value corresponding each of the components represents the amount tobe coated with the unit of g/m². Further, the other value in regard tothe silver halide represents the coating amount in terms of silver.

First Layer (First Halation Preventing Layer) Black colloidal silverSilver 0.122 Silver iodobromide emulsion (0.07 μm) Silver 0.01 Gelatin0.919 ExM-1 0.066 ExC-1 0.002 ExC-3 0.002 Cpd-2 0.001 F-8 0.001 HBS-10.050 HBS-2 0.002

Second Layer (Second Halation Preventing Layer) Black colloidal silverSilver 0.055 Gelatin 0.425 ExF-1 0.002 F-8 0.001 Solid dispersion dyeExF-7 0.120 HBS-1 0.074

Third Layer (Intermediate Layer) ExC-2 0.050 Cpd-1 0.090 Polyethylacrylate latex 0.200 HBS-1 0.100 Gelatin 0.700

Fourth layer (Low-Speed Red Light-Sensitive Emulsion Layer) Em-D Silver0.577 Em-C Silver 0.347 ExC-1 0.188 ExC-2 0.011 ExC-3 0.075 ExC-4 0.121ExC-5 0.010 ExC-6 0.007 ExC-8 0.050 ExC-9 0.020 Cpd-2 0.025 Cpd-4 0.025UV-2 0.047 UV-3 0.086 UV-4 0.018 HBS-1 0.245 HBS-5 0.038 Gelatin 0.994

Fifth Layer (Medium-Speed Red Light-Sensitive Emulsion Layer) Em-BSilver 0.431 Em-C Silver 0.432 ExC-1 0.154 ExC-2 0.068 ExC-3 0.018 ExC-40.103 ExC-5 0.023 ExC-6 0.010 ExC-8 0.016 ExC-9 0.005 Cpd-2 0.036 Cpd-40.009 Cpd-7 0.082 HBS-1 0.129 Gelatin 0.882

Sixth Layer (High-Speed Red Light-Sensitive Emulsion Layer) Em-A Silver1.108 ExC-1 0.180 ExC-3 0.035 ExC-6 0.029 ExC-8 0.110 ExC-9 0.020 Cpd-20.064 Cpd-4 0.008 Cpd-7 0.028 HBS-1 0.329 HBS-2 0.120 Gelatin 1.245

Seventh Layer (Intermediate Layer) Cpd-1 0.094 Cpd-6 0.369 Soliddispersion dye ExF-4 0.030 HBS-1 0.049 Polyethyl acrylate latex 0.088Gelatin 0.886

Eighth Layer (Layer which gives an Interlayer Effect to Red LightSensitive Layer) Em-J Silver 0.153 Em-K Silver 0.153 Cpd-4 0.030 ExM-20.120 ExM-3 0.016 ExM-4 0.026 ExY-1 0.016 ExY-4 0.036 ExC-7 0.026 HBS-10.218 HBS-3 0.003 HBS-5 0.030 Gelatin 0.610

Ninth Layer (Low-Speed Green Light-Sensitive Emulsion Layer) Em-H Silver0.333 Em-G Silver 0.329 Em-I Silver 0.088 ExM-2 0.378 ExM-3 0.047 ExY-10.017 ExC-7 0.007 HBS-1 0.098 HBS-3 0.010 HBS-4 0.077 HBS-5 0.548 Cpd-50.010 Gelatin 1.470

Tenth Layer (Medium-Speed Green Light-Sensitive Emulsion Layer) Em-FSilver 0.457 ExM-2 0.032 ExM-3 0.029 ExM-4 0.029 ExY-3 0.007 ExC-6 0.010ExC-7 0.012 ExC-8 0.010 HBS-1 0.065 HBS-3 0.002 HBS-4 0.020 HBS-5 0.020Cpd-5 0.004 Gelatin 0.446

Eleventh Layer (High-Speed Green Light-Sensitive Emulsion Layer) Em-ESilver 0.794 ExC-6 0.002 ExC-8 0.010 ExM-1 0.013 ExM-2 0.011 ExM-3 0.030ExM-4 0.017 ExY-3 0.003 Cpd-3 0.004 Cpd-4 0.007 Cpd-5 0.010 HBS-1 0.148HBS-3 0.003 HBS-4 0.020 HBS-5 0.037 Polyethyl acrylate latex 0.099Gelatin 0.939

Twelfth Layer (Yellow Filter Layer) Cpd-1 0.094 Solid dispersion dyeExF-2 0.070 Solid dispersion dye ExF-5 0.010 Oil-soluble dye ExF-6 0.010HBS-1 0.049 Gelatin 0.630

Thirteenth Layer (Low-Speed Blue Light-Sensitive Emulsion Layer) Em-OSilver 0.112 Em-M Silver 0.300 Em-N Silver 0.260 ExC-1 0.027 ExC-7 0.013ExY-1 0.002 ExY-2 0.890 ExY-4 0.058 Cpd-2 0.100 Cpd-3 0.004 HBS-1 0.222HBS-5 0.074 Gelatin 1.553

Fourteenth Layer (High-Speed Blue Light-Sensitive Emulsion Layer) Em-LSilver 0.714 ExY-2 0.211 ExY-4 0.068 Cpd-2 0.075 Cpd-3 0.001 HBS-1 0.124Gelatin 0.678

Fifteenth Layer (First Protective Layer) Silver iodobromide emulsion(0.07 μm) Silver 0.301 UV-1 0.211 UV-2 0.132 UV-3 0.198 UV-4 0.026 F-110.009 S-1 0.086 HBS-1 0.175 HBS-4 0.050 Gelatin 1.984

Sixteenth Layer (Second Protective Layer) H-1 0.400 B-1 (diameter: 1.7μm) 0.050 B-2 (diameter: 1.7 μm) 0.150 B-3 0.050 S-1 0.200 Gelatin 0.750

In addition to the above ingredients, in order to improve storagestability, processing suitability, resistance to pressure,mildew-proofing property, bacteria-proofing property, antistaticproperty and coating property, the individual layer properly containedW-1 to W-6, B-4 to B-6, F-1 to F-18, lead salts, platinum salts, iridiumsalts and rhodium salts.

(Preparation of Dispersion of Organic Solid Dispersed Dye)

ExF-2 in the 12th layer was dispersed by the following method. Wet cakeof Ex2-F (containing 2.800 kg 17.6 mass % of water) Sodiumoctylphenyldiethoxymethane 0.376 kg sulfonate (31 mass % aqueoussolution) F-15 (7% aqueous solution) 0.011 kg Water 4.020 kg Total 7.210kg(The pH of the mixture is adjusted to 7.2 with NaOH)(The pH of the Mixture is Adjusted to 7.2 with NaOH)

The slurry having the above-described composition was roughly dispersedwith stirring by a dissolver stirrer, and then dispersed by an agitatormill LMK-4 (trade name) under the conditions of round speed: 10 m/s;discharge amount: 0.6 kg/min; filling rate of zirconia beads having agrain size of 0.3 μm: 80%, until specific absorbance of the dispersionsolution became 0.29. Thus, a dispersion of solid fine particles wasobtained. An average particle diameter of the dye fine particles was0.29 μm.

Similarly, solid dispersions of ExF-4 and ExF-7 were obtained. Theaverage particle diameter of these dye particles was 0.28 μm and 0.49μm, respectively. EXF-5 was dispersed according to the microprecipitation dispersion method described in Example 1 of EuropeanPatent No. 549,489 A. An average particle diameter of the dye fineparticles was 0.06 μm. TABLE 2 Average amount Thick- of Sphere- Circle-ness iodine equivalent equivalent of Name of (mole diameter*¹ Aspectdiameter*² grain Emulsion %) (μm) ratio (μm) (μm) Shape Em-A 4 0.92 14 20.14 Tabular Em-B 5 0.8 12 1.6 0.13 Tabular Em-C 4.7 0.51 7 0.85 0.12Tabular Em-D 3.9 0.37 2.7 0.4 0.15 Tabular Em-E 5 0.92 14 2 0.14 TabularEm-F 5.5 0.8 12 1.6 0.13 Tabular Em-G 4.7 0.51 7 0.85 0.12 Tabular Em-H3.7 0.49 3.2 0.58 0.18 Tabular Em-I 2.8 0.29 1.2 0.27 0.23 Tabular Em-J5 0.8 12 1.6 0.13 Tabular Em-K 3.7 0.47 3 0.53 0.18 Tabular Em-L 5.5 1.49.8 2.6 0.27 Tabular Em-M 8.8 0.64 5.2 0.85 0.16 Tabular Em-N 3.7 0.374.6 0.55 0.12 Tabular Em-O 1.8 0.19 — — — Cubic(Note)*¹A diameter of a sphere whose volume is equivalent to the volume of anindividual grain.*²A diameter of a circle whose area is equivalent to the projected areaof an individual grain.

In Table 2, emulsions Em-A to Em-C were spectrally sensitized by addingan optimal amount of each of spectrally sensitizing dyes 1 to 3,respectively, and they were also optimally gold-sensitized,sulfur-sensitized and selenium-sensitized. Emulsions Em-E to Em-G werespectrally sensitized adding an optimal amount of each of spectrallysensitizing dyes 4 to 6, respectively, and they were also optimallygold-sensitized, sulfur-sensitized and selenium-sensitized. EmulsionEm-J was spectrally sensitized adding an optimal amount of each ofspectrally sensitizing dyes 7 to 8, respectively, and further optimallygold-sensitized, sulfur-sensitized and selenium-sensitized. EmulsionEm-L was spectrally sensitized adding an optimal amount of each ofspectrally sensitizing dyes 9 to 11, respectively, and further optimallygold-sensitized, sulfur-sensitized and selenium-sensitized. EmulsionEm-O was spectrally sensitized adding an optimal amount of each ofspectrally sensitizing dyes 10 to 12, respectively, and furtheroptimally gold-sensitized and sulfur-sensitized. Emulsions Em-D, Em-H,Em-I, Em-K, Em-M, and Em-N were spectrally sensitized adding an optimalamount of each of spectrally sensitizing dyes shown in Table 3,respectively, and they were also optimally gold-sensitized,sulfur-sensitized and selenium-sensitized. TABLE 3 Name of Added amountEmulsion Sensitizing dye (mol/mol Ag) Em-D Sensitizing dye 1 5.44 × 10⁻⁴Sensitizing dye 2 2.35 × 10⁻⁴ Sensitizing dye 3 7.26 × 10⁻⁶ Em-HSensitizing dye 8 6.52 × 10⁻⁴ Sensitizing dye 13 1.35 × 10⁻⁴ Sensitizingdye 6 2.48 × 10⁻⁵ Em-I Sensitizing dye 8 6.09 × 10⁻⁴ Sensitizing dye 131.26 × 10⁻⁴ Sensitizing dye 6 2.32 × 10⁻⁵ Em-K Sensitizing dye 7 6.27 ×10⁻⁴ Sensitizing dye 8 2.24 × 10⁻⁴ Em-M Sensitizing dye 9 2.43 × 10⁻⁴Sensitizing dye 10 2.43 × 10⁻⁴ Sensitizing dye 11 2.43 × 10⁻⁴ Em-NSensitizing dye 9 3.28 × 10⁻⁴ Sensitizing dye 10 3.28 × 10⁻⁴ Sensitizingdye 11 3.28 × 10⁻⁴

The sensitizers in Table 3 are shown below.

In the preparation of tabular grains, low molecular gelatin was usedaccording to the working examples in JP-A-1-158426.

Emulsions Em-A to Em-K each contained an optimal amount of each of Irand Fe.

Emulsions Em-L to Em-O each were reduction-sensitized at the time ofgrain formation.

In the tabular grains, dislocation lines as described in JP-A-3-237450were observed by means of high-pressure electron microscope.

In Emulsions Em-A to Em-C and Em-J, an iodide ion-releasing agent wasused to introduce the dislocation according to the working examples inJP-A-6-11782.

In Emulsion E, silver iodide fine grains that were prepared just beforeaddition in a separate chamber installed with a magnetic couplinginduction type stirrer described in JP-A-10-43570, were used tointroduce the dislocation.

The compounds that were used in each layer, are shown below.

The above-described silver halide color photographic light-sensitivematerial was named sample 101.

Processing was performed using an automatic processor FP-360 B (tradename) available from Fuji Photo Film Co., Ltd. according to thefollowing steps. Note that the processor was remodeled so that theoverflow from the bleaching bath was not introduced to the subsequentbath, but entirely discharged to a waste tank. Note that this FP-360 Bwas installed with an evaporation correction means described in JIIITechnical Disclosure No. 94-4992 (published by Japan Institute ofInvention & Innovation).

Processing steps and processing solution compositions are presentedbelow.

(Processing Steps) (Processing Steps) Processing Processing ProcessingTank step time temperature Replenisher* Volume Color  3 min 5 sec 37.8°C. 20 ml 11.5 l   developing Bleaching 50 sec 38.0° C.  5 ml 5 l Fixing(1) 50 sec 38.0° C. — 5 l Fixing (2) 50 sec 38.0° C.  8 ml 5 l Washing30 sec 38.0° C. 17 ml 3 l Stabilizing (1) 20 sec 38.0° C. — 3 lStabilizing (2) 20 sec 38.0° C. 15 ml 3 l Drying  1 min 30 sec 60.0° C.*The replenishment rate is represented by a value per 1.1 m of a 35 mmwide light-sensitive material sample (equivalent to one 24-exposurefilm)

The stabilizer and fixer were made in a counter-flow system from (2) to(1), and the overflow of washing water was entirely introduced to thefixing bath (2). Note that the amount of the developer carried over tothe bleaching step, the amount of the bleaching solution carried over tothe fixing step, and the amount of the fixer carried over to the washingstep were 2.5 ml, 2.0 ml, and 2.0 ml, respectively, per 1.1 m of a 35 mmwide light-sensitive material. Note also the preceding each crossovertime was 6 sec, and this time was included in the processing time of thepreceding processing step.

The aperture area of the above processor was 100 cm² for the colordeveloper, 120 cm² for the bleaching solution, and approximately 100 cm²for other solutions.

The composition of each processing solution was as follows,respectively: (Color-developer) Tank solution Replenisher (g) (g)Diethylenetriaminepentaacetic acid 3.0 3.0 Disodiumcatechol-3,5-disulfonate 0.3 0.3 Sodium sulfite 3.9 5.3 Potassiumcarbonate 39.0 39.0 Disodium-N,N-bis(2-sulfonatoethyl) 1.5 2.0hydroxylamine Potassium bromide 1.3 0.3 Potassium iodide 1.3 mg —4-Hydroxy-6-methyl-1,3,3a,7-tetrazaindene 0.05 — Hydroxylamine sulfate2.4 3.3 2-Methyl-4-[N-ethyl-N-(β-hydroxyethyl) 4.5 6.5 amino]-anilinesulfonate Water to make 1.0 liter 1.0 liter pH 10.05 10.18(pH was adjusted by potassium hydroxide and sulfuric acid.)

(Bleaching solution) Tank solution Replenisher (g) (g)1,3-Diaminopropanetetraacetic acid 113 170 iron (III) ammoniummonohydrate Ammonium bromide 70 105 Ammonium nitrate 14 21 Succinic acid34 51 Maleic acid 28 42 Water to make 1.0 liter 1.0 liter pH 4.6 4.0(pH was adjusted by aqueous ammonia.)(Fixing (1) Tank Solution)

A mixed solution of the above bleaching tank solution and the belowshown fixing tank solution in the ratio of 5:95 (volume ratio).

(pH 6.8) (Fixing (2)) Tank solution Replenisher (g) (g) Aqueous ammoniumthiosulfate solution 240 ml 720 ml (750 g/liter) Imidazole 7 21 Ammoniummethanethiosulfonate 5 15 Ammonium methanesulfinate 10 30Ethylenediaminetetraacetic acid 13 39 Water to make 1.0 liter 1.0 literpH 7.4 7.45(pH was adjusted by aqueous ammonia and acetic acid)

(pH was adjusted by aqueous ammonia and acetic acid)

(Washing Water)

Tap water was treated by passage through a mixed bed ion-exchange columnfilled with an H-type strong acidic cation exchange resin (AmberliteIR-120B, trade name, made by Rohm & Haas) and an OH-type strong basicanion exchange resin (Amberlite IR-400, the same as the above) so thatthe concentrations of Ca ions and Mg ions in water were both made todecrease to 3 mg/liter or below, followed by adding 20 mg/liter ofsodium dichlorinated isocyanurate and 150 mg/liter of sodium sulfate.The pH of this water was in the range of 6.5 to 7.5.

(Stabilizing Solution) (Stabilizing solution) (Both of tank solution andreplenisher) (g) Sodium p-toluenesulfinate 0.03Polyoxyethylene-p-monononylphenylether 0.2 (av. polymerization degree:10) Sodium 1,2-benzoisothiazoline-3-one 0.10 Disodiumethylenediaminetetraacetate 0.05 1,2,4-Triazole 1.31,4-Bis(1,2,4-triazole-1-ylmethyl)piperazine 0.75 Water to make 1.0liter pH 8.5

Samples 102 to 115 were prepared in the same manner as in Sample 101,except that ExY-2 in the 13th and 14th layers was replaced by thecompound as shown in Table 4. Then, the samples were stored at 25° C.with RH (relative humidity) 65% for 7 days. These samples were used tobe evaluated in the following performances (characteristics).

(Evaluation 1 Calculation of Dmax(UV)/Dmin(V))

A sample subjected to exposure to white light at a color temperature of4,800° K through a sharp cut filter SC-39 (trade name, manufactured byFuji Photo Film Co., Ltd.) for an exposure time of 1 second at aquantity of exposure light of 2,000 CMS and a nonexposed sample wereeach subjected to the color development processing as described above.These two samples, exposed and nonexposed, were measured for colordensity. Of the values obtained, the one measured for the sample havinghigher color density (in this Example, the exposed sample) was definedas Dmax, and the one measured for the sample having a lower colordensity (in this Example, the nonexposed sample) was defined as Dmin. Byusing 10 cm² of each sample after the processing, the gelatin in thephotographic constituent layer was enzymatically decomposed with 20 mlof water containing 5 mg of actinase at 40° C. for 60 minutes to elutethe photographic constituent layer. After cooling the eluate at 25° C.,it was treated with 20 ml of ethyl acetate to extract oil-solublecomponents. The extract was once dried up by use of a rotary evaporatorunder the conditions of 40° C. under reduced pressure, and the finalamount of the extract was made to be 10 ml with ethyl acetate containing0.3% mass of acetic acid in a volumetric flask. The operations ofpreparing a solution from the enzymatic decomposition by actinase tothis were performed under light-shielded conditions. This solution wasmeasured for absorption spectra at 340 nm to 450 nm in a 1-cm thicksilica cell and Dmax(UV))/Dmin(UV) defined below was determined bycalculation.

Definition of Dmax(UV)/Dmin(UV); “the smallest value in a range ofwavelength UV, in which UV is a wavelength within the range of 340 nm ormore and 450 nm or less, among values represented by (an absorbance at awavelength UV, for a portion having the yellow maximum colordensity)/(an absorbance at the wavelength UV, for a portion having theyellow minimum color density).”

(Evaluation 2 Calculation of (B−C)/A)

By using the samples used in Evaluation 1, the yellow density B at theportion showing the maximum color density (Dmax) (that is, in thisExample, of the exposed sample) and the yellow density C at the portionshowing the minimum color density (Dmin) (that is, in this Example, ofthe nonexposed sample) were measured by use of an SCD meter. (B−C)/A isdetermined by calculation by using the coating amount of the compoundrepresented by the formula (I), namely A mol/m².

(Evaluation 3 Static-Induced Fog)

Each sample was processed into a roll and rewound at a rate of 100m/minute in an atmosphere of 25° C. and a relative humidity of 10% inthe absence of light, and then the above-mentioned developmentprocessing step was performed without exposure to light. The number ofstatic-induced fogs that occurred in the sample (Dmin) after theprocessing was visually detected. Relative values (%) relative to thenumber of static-induced fogs occurring in Sample 101 are shown in Table4 below TABLE 4 Coupler in Static- 13th Coupler in 14th Dmax(UV)/induced No. layer (##) layer (##) Dmin(UV) (B − C)/A fog 101 ExY-2 ExY-21.15 — 100 102 (31) ExY-2 0.87 2600 60 103 (33) ExY-2 0.85 2500 50 104(34) ExY-2 0.86 2650 55 105 (39) ExY-2 0.78 2580 51 106 (40) ExY-2 0.752580 49 107 (33) (31) 0.6 2270 30 108 (33) (33) 0.62 2300 33 109 (35)(35) 0.64 2200 35 110 (36) (36) 0.65 2080 36 111 (37) (37) 0.66 2100 34112 (39) (39) 0.62 2200 31 113 (40) (40) 0.55 2200 32 114 ExY-2/(39)(39) 0.89 3800 59 *1 115 ExY-2/(40) ExY-2/(40) *2 0.9 8900 70 *2(##) When replacing ExY-2 with the coupler according to the presentinvention, the amount of the coupler according to the present inventionwas 0.8 times that of ExY-2 in terms of mole.*1) 50:40 mixture (molar ratio assuming that the amount of ExY-2 inSample 101 is made up to 100)*2) 75:20 mixture (molar ratio assuming that the amount of ExY-2 inSample 101 is made up to 100)

From Table 4 above, it can be seen that the photosensitive material ofthe present invention is apparently excellent in static-induced fog.

Example 1-2

As shown in Table 5, samples prepared in the same manner as in Example1-1 except that the 15^(th) layer was changed in each sample of Example1-1 as described below were subjected to Evaluations 1, 2 and 3 as inExample 1-1 as well as the following evaluation. Also, the sampledescribed in JP-A-6-130549 was subjected to the same evaluations.

15^(th) Layer (First Protective Layer) 0.07-μm Silver iodobromideemulsion Silver 0.301 UV-1 0.175 UV-2 0.110 UV-3 0.164 UV-4 0.022 F-110.009 S-1 0.086 HBS-1 0.175 HBS-4 0.050 Gelatin 1.647(Evaluation 4 Evaluation of Sharpness)

By using the above-mentioned sample, a pattern for evaluating MTF waswritten by exposure to white light and then the above-mentioned colordevelopment processing was performed in the same manner. The sharpnessof magenta density is shown in a relative value relative to that ofSample 101. The greater the numerical value is, the higher the sharpnessis, which is more preferred. TABLE 5 Sample No. in Static- Example 1-1which Modification in Dmax(UV)/ induced No. was to be modified 15thlayer Dmin(UV) (B − C)/A fog Sharpness G 101 101 Not modified 1.15 — 1001.00 108 108 Not modified 0.62 2300 33 1.20 201 101 Modified 1.15 — 1301.15 202 108 Modified 0.62 2300 70 1.28 203 109 Modified 0.64 2200 751.30 204 112 Modified 0.62 2200 82 1.25 206 113 Modified 0.55 2200 731.27  207* — — 1.17 — 105 1.02  208* — — 1.17 — 107 1.01*Samples described in Table 1 of Example 1 in JP-A-6-130549

From Table 5, it can be seen clearly that the silver halide photographicsensitive material of the present invention is excellent instatic-induced fog and in sharpness.

Example 1-3

Samples prepared in Example 1-1 and Example 1-2 were processed into aroll of a width of 35 mm, packed into a patrone and subjected to camerapassing tests under the conditions of a relative humidity of 10% androom temperature (25° C.) by feeding the film at a high speed. Thesamples were processed by the above-mentioned development processing andthen evaluated on fog, respectively. As a result, samples that werefound to be effective to static-induced fog in Examples 1-1 and 1-2showed no fogs.

Example 1-4 (Preparation of Sample having Multilayers) Preparation ofSilver Halide Color Photographic Light-Sensitive Material, Sample CR01

(i) Coating of Backing Layers

The following backing layers were coated on one side oftriacetylcellulose having the thick of 205 μm support provided withundercoat on both sides.

First Layer Binder: acid-processed gelatin 1.00 g (isoelectric point9.0) Polymer latex P-2 0.13 g (av. particle diameter 0.1 μm) Polymerlatex P-3 0.23 g (av. particle diameter 0.2 μm) Ultraviolet rayabsorbent U-1 0.030 g Ultraviolet ray absorbent U-3 0.010 g Ultravioletray absorbent U-4 0.020 g High-boiling organic solvent Oil-2 0.030 gSurface active agent W-3 0.010 g Surface active agent W-6 3.0 mg

Second Layer Binder: acid-processed gelatin 3.10 g (isoelectric point9.0) Polymer latex: P-3 0.11 g (av. particle diameter 0.2 μm)Ultraviolet ray absorbent U-1 0.030 g Ultraviolet ray absorbent U-30.010 g Ultraviolet ray absorbent U-4 0.020 g High-boiling organicsolvent Oil-2 0.030 g Surface active agent W-3 0.010 g Surface activeagent W-6 3.0 mg Dye D-2 0.10 g Dye D-10 0.12 g Potassium sulfate 0.25 gCalcium chloride 0.5 mg Sodium hydroxide 0.03 g

Third Layer Binder: acid-processed gelatin 3.30 g (isoelectric point9.0) Surface active agent W-3 0.020 g  Potassium sulfate 0.30 g Sodiumhydroxide 0.03 g

Fourth Layer Binder: lime-processed gelatin  1.15 g (isoelectric point5.4) Copolymer of methacrylic acid and 0.040 g methyl methacrylate (1:9)(av. particle diameter, 2.0 μm) Copolymer of methacrylic acid and 0.030g methyl methacrylate (6:4) (av. particle diameter, 2.0 μm) Surfaceactive agent W-3 0.060 g Surface active agent W-2 0.010 g Hardener H-1 0.23 g(iv) Coating of Light-Sensitive Emulsion Layers

The surface of the support on the side opposite to the backing layer,was coated with light-sensitive emulsion layers having the followingcompositions to produce a sample CR01. The number corresponding to eachingredient indicates the addition amount per m². Note that the effect ofthe compound added is not limited to the use of the compound describedbelow.

First layer: Anti-Halation Layer Black colloidal silver 0.20 g Gelatin2.50 g Compound Cpd-B 0.050 g Ultraviolet absorber U-1 0.050 gUltraviolet absorber U-3 0.10 g Ultraviolet absorber U-4 0.030 gUltraviolet absorber U-5 0.050 g Ultraviolet absorber U-7 0.10 gCompound Cpd-F 0.20 g High boiling organic solvent Oil-1 0.10 g Highboiling organic solvent Oil-2 0.15 g High boiling organic solvent Oil-50.010 g Dye D-4 1.0 mg Dye D-8 2.5 mg Fine crystal solid dispersion ofDye E-1 0.05 g

Second Layer: Intermediate Layer Gelatin 1.8 g Compound Cpd-M 0.20 gCompound Cpd-F 0.050 g Compound Cpd-K 3.0 mg Ultraviolet absorber U-66.0 mg High boiling organic solvent Oil-3 0.010 g High boiling organicsolvent Oil-4 0.010 g High boiling organic solvent Oil-6 0.10 g Highboiling organic solvent Oil-7 2.0 mg Dye D-7 4.0 mg

Third Layer: Intermediate Layer Gelatin  0.40 g Compound Cpd-D 0.020 gHigh boiling organic solvent Oil-3 0.010 g High boiling organic solventOil-8 0.010 g

Forth Layer: Low-Sensitivity Red-Sensitive Emulsion Layer Emulsion ASilver 0.15 g Emulsion B Silver 0.15 g Emulsion C Silver 0.15 g Gelatin0.80 g Coupler C-1 0.10 g Coupler C-2 7.0 mg Coupler C-10 2.0 mgUltraviolet absorber U-3 0.010 g Compound Cpd-I 5.0 mg Compound Cpd-D3.0 mg Compound Cpd-J 2.0 mg High boiling organic solvent Oil-10 0.030 gAdditive P-1 5.0 mg

Fifth Layer: Middle-Sensitivity Red-Sensitive Emulsion Layer Emulsion CSilver 0.15 g Emulsion D Silver 0.15 g Silver bromide emulsion, withinner Silver 3.0 mg part of which was fogged (cube, av.sphere-equivalent diameter of 0.11 μm) Gelatin 0.70 g Coupler C-1 0.15 gCoupler C-2 7.0 mg Compound Cpd-D 3.0 mg Ultraviolet absorber U-3 0.010g High boiling organic solvent Oil-10 0.030 g Additive P-1 7.0 mg

Sixth Layer: High-Sensitivity Red-Sensitive Emulsion Layer Emulsion ESilver 0.20 g Emulsion F Silver 0.20 g Gelatin 1.50 g Coupler C-1 0.60 gCoupler C-2 0.025 g Coupler C-3 0.020 g Coupler C-9 5.0 mg Ultravioletabsorber U-1 0.010 g Ultraviolet absorber U-2 0.010 g High boilingorganic solvent Oil-6 0.030 g High boiling organic solvent Oil-9 0.020 gHigh boiling organic solvent Oil-10 0.20 g Compound Cpd-D 5.0 mgCompound Cpd-K 1.0 mg Compound Cpd-F 0.030 g Compound Cpd-L 1.0 mgCompound Cpd-R 0.030 g Additive P-1 0.010 g Additive P-4 0.030 g

Seventh Layer: Intermediate Layer Gelatin 0.60 g Additive P-2 0.10 g DyeD-5 0.020 g Dye D-9 6.0 mg Compound Cpd-I 0.010 g Compound Cpd-O 3.0 mgCompound Cpd-P 5.0 mg High boiling organic solvent Oil-6 0.050 g

Eighth Layer: Intermediate Layer Yellow colloidal silver Silver 0.010 gGelatin 1.30 g Additive P-2 0.05 g Ultraviolet absorber U-1 0.010 gUltraviolet absorber U-2 0.030 g Compound Cpd-A 0.050 g Compound Cpd-D0.030 g Compound Cpd-M 0.10 g High boiling organic solvent Oil-3 0.010 gHigh boiling organic solvent Oil-6 0.10 g

Ninth Layer: Low-Sensitivity Green-Sensitive Emulsion layer Emulsion GSilver 0.15 g Emulsion H Silver 0.30 g Emulsion I Silver 0.15 g Gelatin1.30 g Coupler C-4 0.10 g Coupler C-5 0.030 g Compound Cpd-A 5.0 mgCompound Cpd-B 0.020 g Compound Cpd-G 2.5 mg Compound Cpd-F 0.010 gCompound Cpd-K 2.0 mg High boiling organic solvent Oil-2 0.040 gAdditive P-1 5.0 mg

Tenth Layer: Middle-Sensitivity Green-Sensitive Emulsion layer EmulsionI Silver 0.20 g Emulsion J Silver 0.20 g Silver bromide emulsion, withinner Silver 3.0 mg part of which was fogged (cube, av.sphere-equivalent diameter of 0.11 μm) Gelatin 0.50 g Coupler C-4 0.15 gCoupler C-5 0.050 g Coupler C-6 0.010 g Compound Cpd-A 5.0 mg CompoundCpd-B 0.020 g High boiling organic solvent Oil-2 0.020 g

Eleventh Layer: High-Sensitivity Green-Sensitive Emulsion layer EmulsionK Silver 0.40 g Gelatin 1.20 g Coupler C-4 0.50 g Coupler C-5 0.20 gCoupler C-7 0.050 g Compound Cpd-B 0.030 g Compound Cpd-F 0.010 g Highboiling organic solvent Oil-2 0.050 g High boiling organic solvent Oil-90.020 g

Twelfth Layer: Yellow Filter Layer Yellow colloidal silver Silver 5.0 mgGelatin 1.0 g Compound Cpd-C 0.010 g Compound Cpd-M 0.030 g High boilingorganic solvent Oil-1 0.020 g High boiling organic solvent Oil-6 0.040 gFine crystal solid dispersion of Dye E-2 0.20 g Thirteenth layer:Intermediate layer Gelatin 0.40 g Compound Cpd-Q 0.20 g Dye D-6 4.0 mg

Fourteenth Layer: Low-Sensitivity Blue-Sensitive Emulsion layer EmulsionL Silver 0.15 g Emulsion M Silver 0.10 g Emulsion N Silver 0.10 gGelatin 0.80 g Coupler C-8 0.30 g Compound Cpd-B 0.10 g Compound Cpd-I8.0 mg Compound Cpd-K 1.0 mg Ultraviolet absorber U-6 0.010 g Highboiling organic solvent Oil-2 0.010 g

Fifteenth Layer: Middle-Sensitivity Blue-Sensitive Emulsion LayerEmulsion N Silver 0.10 g Emulsion O Silver 0.20 g Gelatin 0.80 g CouplerC-8 0.30 g Compound Cpd-B 0.10 g Compound Cpd-E 0.030 g Compound Cpd-N2.0 mg High boiling organic solvent Oil-2 0.010 g

Sixteenth Layer: High-Sensitivity Blue-Sensitive Emulsion Layer EmulsionP Silver 0.20 g Emulsion Q Silver 0.25 g Gelatin 2.00 g Coupler C-8 1.40g Coupler C-2 0.010 g High boiling organic solvent Oil-2 0.030 gUltraviolet absorber U-6 0.10 g Compound Cpd-E 0.20 g Compound Cpd-N 5.0mg

Seventeenth Layer: First Protective Layer Gelatin 1.00 g Ultravioletabsorber U-1 0.10 g Ultraviolet absorber U-2 0.050 g Ultravioletabsorber U-5 0.10 g Ultraviolet absorber U-7 0.10 g Compound Cpd-B 0.020g Compound Cpd-O 5.0 mg Compound Cpd-A 0.030 g Compound Cpd-H 0.20 g DyeD-1 8.0 mg Dye D-2 0.010 g Dye D-3 0.010 g High boiling organic solventOil-3 0.10 g

Eighteenth Layer: Second Protective Layer Colloidal silver Silver 2.5 mgFine grain silver iodobromide emulsion Silver 0.10 g (av. grain diameterof 0.06 μm, AgI content of 1 mol %) Gelatin 0.80 g Ultraviolet absorberU-1 0.030 g Ultraviolet absorber U-6 0.030 g High boiling organicsolvent Oil-3 0.010 g

Nineteenth Layer: Third Protective Layer Gelatin 1.00 g Polymethylmethacrylate 0.10 g (av. particle diameter of 1.5 μm) Copolymer ofmethyl methacrylate and 0.15 g methacrylic acid (6:4) (av. particlediameter, 1.5 μm) Silicone oil SO-1 0.20 g Surface active agent W-1 3.0mg Surface active agent W-2 8.0 mg Surface active agent W-3 0.040 gSurface active agent W-7 0.015 g

Further, to all emulsion layers, in addition to the above-describedcomponents, additives F-1 to F-9 were added. Further, to each layer, inaddition to the above-described components, a gelatin hardener H-1 andsurface active agents W-3, W-4, W-5, and W-6 for coating andemulsifying, were added.

Further, as antifungal and antibacterial agents, phenol,1,2-benzisothiazoline-3-one, 2-phenoxyethanol, phenetylalcohol, andp-hydroxybenzoic acid butyl ester were added. TABLE 6 Constitution forsilver halide emulsion Silver iodobromide emulsions used in Sample 101Average Halogen Agl sphere- Average composition content equivalentVariation Agl structure of at grain diameter coefficient content silverhalide surface Other characteristics Emulsion Characteristics (μm) (%)(%) grains (%) (1) (2) (3) (4) (5) A Monodisperse 0.24 9 3.5 Triple 1.5◯ tetradecahedral structured grains B Monodisperse (111) 0.25 10 3.5Quadruple 1.5 ◯ ◯ ◯ ◯ tabular grains structured Average aspect ratio 3.0C Monodisperse (111) 0.35 19 3.0 Triple 0.1 ◯ ◯ ◯ ◯ tabular grainsstructured Average aspect ratio 4.5 D Monodisperse (111) 0.35 21 4.8Triple 2.0 ◯ ◯ ◯ ◯ tabular grains structured Average aspect ratio 6.0 EMonodisperse (111) 0.45 10 2.0 Quadruple 1.5 ◯ tabular grains structuredAverage aspect ratio 6.0 F Monodisperse (111) 0.60 12 1.6 Triple 0.6 ◯ ◯◯ tabular grains structured Average aspect ratio 8.0 G Monodisperse 0.159 3.5 Quadruple 2.0 ◯ cubic grains structured H Monodisperse 0.24 12 4.9Quadruple 0.1 ◯ ◯ ◯ cubic grains structured I Monodisperse (111) 0.30 123.5 Quintet 4.5 ◯ ◯ ◯ ◯ tabular grains structured Average aspect ratio4.0 J Monodisperse (111) 0.45 21 3.0 Quadruple 0.2 ◯ ◯ ◯ ◯ tabulargrains structured Average aspect ratio 7.0 K Monodisperse (111) 0.60 132.7 Triple 1.3 ◯ ◯ ◯ tabular grains structured Average aspect ratio 8.5L Monodisperse 0.31 9 7.5 Triple 7.0 ◯ ◯ tetradecahedral structuredgains M Monodisperse 0.31 9 7.5 Triple 5.0 ◯ ◯ ◯ tetradecahedralstructured grains N Monodisperse (111) 0.33 13 2.1 Quadruple 4.0 ◯ ◯ ◯tabular grains structured Average aspect ratio 3.0 O Monodisperse (111)0.43 9 2.5 Quadruple 1.0 ◯ ◯ ◯ tabular grains structured Average aspectratio 5.0 P Monodisperse (111) 0.75 21 2.8 Triple 0.5 ◯ ◯ ◯ tabulargrains structured Average aspect ratio 9.0 Q Monodisperse (111) 0.90 81.0 Quadruple 0.5 ◯ ◯ ◯ tabular grains structured Average aspect ratio9.0(Other characteristics above)(1): A reduction sensitizer was added during formation of grains.(2): A selenium sensitizer was used as an after-ripening chemical.(3): A rhodium salt was added during formation of grains.(4): After completion of after-ripening, silver nitrate in an amount of10% in terms of the silver molar ratio relative to the emulsion grainsat the time, and potassium bromide in an equimolar amount to the silvernitrate, were added to form shells.(5): The presence of 10 or more dislocation lines/grain on average wasobserved under a transmission electron microscope.

All the photosensitive emulsions were after-ripened using sodiumthiosulfate, potassium thiocyanate and sodium chloroaurate. Further, aniridium salt was added as necessary during formation of grains.

Chemically modified gelatin whose amino groups had been partiallyconverted into phthalic amide was added to the emulsions B, C, E, H, J,N, Q and R when the emulsions were prepared. TABLE 7 Spectralsensitization of Emulsions A to P Added Added amount per 1 Stage when asensitizing Emulsion sensitizing dye mol of silver halide (g) dye wasadded A S-1 0.01 After afterripening S-2 0.15 Before afterripening S-30.02 Before afterripening S-8 0.03 Before afterripening S-13 0.25 Beforeafterripening S-14 0.01 Before afterripening B S-2 0.15 Beforeafterripening S-3 0.02 Before afterripening S-8 0.03 Beforeafterripening S-13 0.25 Before afterripening S-14 0.01 Beforeafterripening C S-2 0.25 Before afterripening S-8 0.04 Beforeafterripening S-13 0.20 Before afterripening D S-2 0.2 Afterafterripening S-3 0.05 After afterripening S-8 0.05 Before afterripeningS-13 0.25 Before afterripening E S-1 0.01 Before afterripening S-2 0.25Before afterripening S-8 0.05 Before afterripening S-13 0.25 Afterafterripening F S-2 0.2 Before afterripening S-3 0.04 Beforeafterripening S-8 0.20 Before afterripening G S-4 0.3 Afterafterripening S-5 0.05 After afterripening S-12 0.1 After afterripeningH S-4 0.2 Before afterripening S-5 0.05 After afterripening S-9 0.15Before afterripening S-14 0.02 After afterripening I S-4 0.3 Beforeafterripening S-9 0.2 Before afterripening S-12 0.1 Before afterripeningJ S-4 0.35 Before afterripening S-5 0.05 After afterripening S-12 0.1Before afterripening K S-4 0.3 Before afterripening S-9 0.05 Beforeafterripening S-12 0.1 Before afterripening S-14 0.02 Beforeafterripening L, M S-6 0.1 After afterripening S-10 0.2 Afterafterripening S-11 0.05 After afterripening N S-6 0.05 Afterafterripening S-7 0.05 After afterripening S-10 0.25 After afterripeningS-11 0.05 After afterripening O S-10 0.4 After afterripening S-11 0.15After afterripening P S-6 0.05 After afterripening S-7 0.05 Afterafterripening S-10 0.3 Before afterripening S-11 0.1 Beforeafterripening Q S-6 0.05 Before afterripening S-7 0.05 Beforeafterripening S-10 0.2 Before afterripening S-11 0.25 Beforeafterripening C-1

C-2

C-3

C-4

C-5

C-6

C-7

C-8

C-9

C-10

Oil-1 Tri-n-hexyl phosphate Oil-2 Tricresyl phosphate Oil-3

Oil-4 Tricyclohexyl phosphate Oil-5 Bis(2-ethylhexyl)succinate Oil-6

Oil-7

Oil-8

Oil-9

Oil-10

Cpd-A

Cpd-B

Cpd-C

Cpd-D

Cpd-E

Cpd-F

Cpd-G

Cpd-H

Cpd-I

Cpd-J

Cpd-K

Cpd-L

Cpd-M

Cpd-N

Cpd-O

Cpd-P

Cpd-Q

Cpd-R

U-1

U-2

U-3

U-4

U-5

U-6

U-7

S-1

S-2

S-3

S-4

S-5

S-6

S-7

S-8

S-9

S-10

S-11

S-12

S-13

S-14

D-1

D-2

D-3

D-4

D-5

D-6

D-7

D-8

D-9

D-10

E-1

E-2

H-1

W-1

W-2

W-3

W-4

W-5

W-6

W-7 C₈F₁₇SO₃Li P-1

P-2

P-3

P-4

F-1

F-2

F-3

F-4

F-5

F-6

F-7

F-8

F-9

SO-1

Preparation of Dispersion of Organic Solid Dispersed Dye (Preparation ofDispersion of Dye E-1)

To a wet cake of Dye E-1 (the net amount of E-1: 270 g), 100 g ofPluronic F88 (trade name, block copolymer ofethyleneoxide/propyleneoxide) manufactured by BASF and water were addedand stirred. Water was added so as to give a total amount of 4000 g.Next, to the ulutravisco mill (UVM-2 (trade name), manufactured by AIMEXCo., Ltd.) filled with 1700 ml of zirconia beads having an average graindiameter of 0.5 mm, the resultant slurry was added and ground for 2hours under the conditions of about 10 m/sec of round speed and 0.5liter/min of discharge amount. The beads were filtered away to obtain adispersion of the dye. Water was added to the dispersion so that the dyedensity was diluted to 3%. Then, for the purpose of stabilization, thedispersion was heated at 90° C. for 10 hours. An average particlediameter of thus obtained dye fine particles was 0.30 μm. The range ofthe distribution of the particle diameter (standard deviation ofparticle diameter×100/average particle diameter) was 20%.

(Preparation of Solid Dispersion of Dye E-2)

To 1400 g of a wet cake of Dye E-2 containing 30 mass % of water, waterand 270 g of W-4 were added and stirred. Water was added so that aslurry containing 40 mass % of E-2 was obtained. Next, to theulutravisco mill (UVM-2 (trade name), manufactured by AIMEX Co., Ltd.)filled with 1700 ml of zirconia beads having an average grain size of0.5 mm, the resultant slurry was added and ground for 8 hours under theconditions of about 10 m/sec of round speed and 0.5 liter/min ofdischarge amount. Thus, a solid fine particle dispersion of Dye E-2 wasobtained. This dispersion was diluted with an ion exchanged water to 20mass %, to obtain solid fine particle dispersion. Note that the averageparticle size of fine particle dispersion is 0.15 μm.

Then, as shown in Table 8, Samples CR02 to CR07 were prepared bysubstituting the coupler C-8 in the 14^(th), 15^(th) and 16^(th) layersof Sample CR01 by one.

Upon substitution of the coupler, substitution was performed bysubstituting a substitute coupler in a mole number by 0.9 time as muchas that of the coupler C-8 in Sample CR01. Besides this, the additivesother than those particularly indicated were the same as those in SampleCR01.

Note that when the samples were used in the following evaluations, thecoated photosensitive materials were evaluated after they were storedunder the conditions of 25° C. and a relative humidity of 55% for 14days. TABLE 8 Constitution of Samples Sample Coupler in the 14th, 15thand 16th layer CR01 C-8 (As shown in the specification) CR02 (41) CR03(42) CR04 (43) CR05 (46) CR06 (48) CR07 (50)(Evaluation of Samples)(1) Calculation of Dmax(UV)/Dmin(UV)

Two pieces of each of Samples CR01 to CR07 cut into a size of 10.5cm×12.5 cm were prepared. One of them was subjected to exposure to whitelight at a color temperature of 4,800° K through a sharp cut filterSC-39 (trade name, manufactured by Fuji Photo Film Co., Ltd.) for anexposure time of 1 second at a quantity of exposure light of 2,000 CMSand then the following development processing-CR was performed (thewhole surface gave the minimum density; hereinafter referred to as aminimum density sample).

Another piece maintained nonexposed was passed on to the operationsafter the reversal processing only in the development processing-CR (thewhole surface gave the maximum density of the photosensitive material;hereinafter, referred to as a maximum density sample).

The minimum density sample and maximum density sample thus prepared werepunched into small disks in the same manner as described in Example 1-1and the disks were extracted and measured of ultraviolet absorption. Thevalues of Dmax(UV)/Dmin(UV) thus obtained are shown in Table 9.

(2) Evaluation of Static-Induced Fog

Samples CR01 to CR07 were each processed into a roll with a width of12.7 cm×200 m and rewound at a rate of 100 m/minute in an atmosphere of25° C. and a relative humidity of 10% in the absence of light,respectively, and then the development processing step —CR was performedwithout exposure to light (provided that a sensitized developmentprocessing in which the first development time was extended to 13minutes was performed).

The number of static-induced fogs (white areas in the black background)that occurred after the processing was visually detected. Table 9 showsrelative values by taking the number of static-induced fogs occurring inSample CR01 as 1.0. The smaller the numerical value is, the less thestatic-induced fog is, which is more preferred. TABLE 9 Result ofevaluation Dmax(UV)/ Relative ratio of static- Sample Dmin(UV) inducedfog CR01 1.15 1.0 (standard) CR02 0.68 0.4 CR03 0.68 0.4 CR04 0.66 0.3CR05 0.66 0.3 CR06 0.60 0.3 CR07 0.65 0.3

According to Table 9, it is revealed that use of the photosensitivematerial of the present invention results in a remarkably decreasedoccurrence of static-induced fog.

(Processing-CR) Tank Replenisher Processing step Time Temperature volumeamount 1st development 6 min 38° C. 37 liters 2,200 ml/m² 1stwater-washing 2 min 38° C. 16 liters 4,000 ml/m² Reversal 2 min 38° C.17 liters 1,100 ml/m² Color-development 6 min 38° C. 30 liters 2,200ml/m² Pre-bleaching 2 min 38° C. 19 liters 1,100 ml/m² Bleaching 6 min38° C. 30 liters   220 ml/m² Fixing 4 min 38° C. 29 liters 1,100 ml/m²2nd water-washing 4 min 38° C. 35 liters 4,000 ml/m² Final-rinsing 1 min25° C. 19 liters 1,100 ml/m²

Compositions of each processing solution used were as follows:

(1st Developer) Tank solution Replenisher Pentasodium nitrilo-N,N,N- 1.5g 1.5 g trimethylenephosphonate Pentasodium diethylenetriamine- 2.0 g2.0 g pentaacetate Sodium sulfite 30 g 30 g Hydroquinone/potassium 20 g20 g monosulfonate Potassium carbonate 15 g 20 g Sodium bicarbonate 12 g15 g 1-Phenyl-4-methyl-4-hydroxymethyl- 1.5 g 2.0 g 3-pyrazolidonePotassium bromide 2.5 g 1.4 g Potassium thiocyanate 1.2 g 1.2 gPotassium iodide 2.0 mg — Diethylene glycol 13 g 15 g Water to make1,000 ml 1,000 ml pH 9.60 9.60

-   -   (pH was adjusted by using sulfuric acid or potassium hydroxide)        (Reversal Solution)

(Both of tank solution and replenisher) Pentasodium nitrilo-N,N,N- 3.0 gtrimethylenephosphonate Stannous chloride dihydrate 1.0 g p-Aminophenol0.1 g Sodium hydroxide 8 g Glacial acetic acid 15 ml Water to make 1,000ml pH 5.80(pH was adjusted by using acetic acid or sodium hydroxide)

(Color-Developer) Tank solution Replenisher Pentasodium nitrilo-N,N,N-2.0 g 2.0 g trimethylenephosphonate Sodium sulfite 6.0 g 6.0 g Trisodiumphosphate 12-hydrate 22 g 22 g Potassium bromide 1.0 g — Potassiumiodide 30 mg — Sodium hydroxide 12.0 g 12.0 g Citrazinic acid 0.5 g 0.5g N-Ethyl-N-(β-methanesulfonamidoethyl)- 10 g 10 g3-methyl-4-aminoaniline-3/2 sulfate- monohydrate3,6-Dithiaoctane-1,8-diol 0.7 g 0.7 g Water to make 1,000 ml 1,000 ml pH11.90 12.00

-   -   (pH was adjusted by using sulfuric acid or potassium hydroxide)

(Pre-Bleaching Solution) Tank Solution Repleisher Disodiumethylenediaminetetraacetate 8.0 g 8.0 g dihydrate Sodium sulfite 6.0 g8.0 g 1-Thioglycerol 0.4 g 0.4 g Formaldehyde-sodium bisulfite adduct 30g 35 g Water to make 1,000 ml 1,000 ml pH 6.50 6.50

-   -   (pH was adjusted by using acetic acid or sodium hydroxide)

(Bleaching Solution) Tank solution Replenisher Disodiumethylenediaminetetraacetate 2.0 g 4.0 g dihydrate Iron (III) ammoniumethylenediamine- 120 g 240 g tetraacetate dihydrate Potassium bromide100 g 200 g Ammonium nitrate 10 g 20 g Water to make 1,000 ml 1,000 mlpH 5.70 5.50

-   -   (pH was adjusted by using nitric acid or sodium hydroxide)        (Fixing Solution)

(Both of Tank Solution and Replenisher) Ammonium thiosulfate 80 g Sodiumsulfite 5.0 g Sodium bisulfite 5.0 g Water to make 1,000 ml pH 6.60

-   -   (pH was adjusted by using acetic acid or aqueous ammonia)

(Stabilizing Solution) Tank solution Replenisher1,2-Benzoisothiazolin-3-one 0.02 g 0.03 g Polyoxyethylene-p-monononylphenyl ether 0.3 g 0.3 g (av. polymerization degree: 10) Polymaleic acid0.1 g 0.15 g (av. molecular weight 2,000) Water to make 1,000 ml 1,000ml pH 7.0 7.0

In the above-described processing steps, a processing solution wasstirred with a continuous circulation in each bath. The lower part ofeach tank was installed with a bubble-releasing tube having tiny holes(diameter 0.3 mm) made at intervals of 1 cm. The processing solution wasstirred while continuously releasing a nitrogen gas (bubbles) from thisbubble-releasing tube. However, such stirring while releasing bubbleswas not carried out in the pre-bleaching bath and the second washingbath.

Example 1-5 Preparation of Blue-sensitive Layer Emulsion A

Silver halide cubic grains having the following characteristics wereformed.

Halogen composition: AgCl 98.9 mole %, AgBr 1 mole %, AgI 0.1 mole %;Average side length: 0.7 μm; Variation coefficient of side length: 8%.Spectral sensitizing dyes-1 and 2 were added to the silver halideemulsion in an amount of 2.5×10⁻⁴ mole/mole of Ag and 2.0×10⁻⁴ mole/moleof Ag respectively.

At the step of grain formation, K₃IrCl₅(H₂O), K₄Ru(CN)₆, K₄Fe(CN)₆,thiosulfonic acid compound-1, sodium thiosulfate, gold sensitizer-1,mercapto compounds-1 and 2 were used in an optimal amount respectively.Thus, Emulsion A-1 for a high-sensitive layer was prepared.

Similarly, cubic grains having an average side length of 0.55 μm and avariation coefficient of 9% in terms of the side length were formed.

Spectral sensitization and chemical sensitization were performed in thesame manner as the above, except for correcting the sensitizationamounts so as to meet specific surface area (according to the ratio ofthe side lengths 0.7/0.55=1.27 fold), to prepare a blue sensitive layerlow-sensitivity emulsion A-2.

(Preparation of Inventive Green Sensitive Layer Emulsions C-1 and C-2)

Under the same preparation conditions for Emulsions A-1 and A-2 in theabove Emulsion A, except that the temperature at the time of forminggrains was lowered, and that the kind of sensitizing dyes were changedas described below, a green sensitive layer (GL) high-sensitivityemulsion C-1 and a green sensitive layer (GL) low-sensitivity emulsionC-2 were prepared.

As for the grain size, the high-sensitivity emulsion C-1 had the averageside length of 0.40 μm and the low-sensitivity emulsion C-2 had theaverage side length of 0.30 μm, each with the variation coefficient ofaverage length of 8%.

The sensitizing dye D was added to the large-size emulsion(high-sensitivity emulsion C-1) in an amount of 3.0×10⁻⁴ mol, and to thesmall-size emulsion (low-sensitivity emulsion C-2) in an amount of3.6×10⁻⁴ mol, per mol of the silver halide; and the sensitizing dye Ewas added to the large-size emulsion in an amount of 4.0×10⁻⁵ mol, andto the small-size emulsion in an amount of 7.0×10⁻⁵ mol, per mol of thesilver halide.

(Preparation of Inventive Red Sensitive Layer Emulsions E-1 and E-2)

Under the same preparation conditions for Emulsions A-1 and A-2 in theabove Emulsion A, except that the temperature at the time of forminggrains was lowered, and the kind of sensitizing dyes were changed asdescribed below, a red sensitive layer high-sensitivity emulsion E-1 anda red sensitive layer low-sensitivity emulsion E-2 were prepared.

As for the grain size, the high-sensitivity emulsion E-1 had the averageside length of 0.38 μm and the low-sensitivity emulsion E-2 had theaverage side length of 0.32 μm, with the variation coefficient ofaverage length of 9% and 10%, respectively.

(The sensitizing dye G and H was added to the large-size emulsion(high-sensitivity emulsion E-1) in an amount of 8.0×10⁻⁵ mol, and to thesmall-size emulsion (low-sensitivity emulsion E-2) in an amount of10.7×10⁻⁵ mol, per mol of the silver halide, respectively.

Further, Compound I below was added to red sensitive layer in an amountof 3.0×10⁻³ mol per mol of a silver halide.)

(Preparation of a Coating Solution for the First Layer)

Into 21 g of a solvent (Solv-1) and 80 ml of ethyl acetate weredissolved 57 g of a yellow coupler (ExY), 7 g of a color-imagestabilizer (Cpd-1), 4 g of a color-image stabilizer (Cpd-2), 7 g of acolor-image stabilizer (Cpd-3), and 2 g of a color-image stabilizer(Cpd-8). This solution was emulsified and dispersed in 220 g of a 23.5mass % aqueous gelatin solution containing 4 g of sodiumdodecylbenzenesulfonate with a high-speed stirring emulsifier(dissolver). Water was added thereto, to prepare 900 g of an emulsifieddispersion A.

On the other hand, the above emulsified dispersion A and the prescribedemulsions A-1 and A-2 were mixed and dissolved, and the first-layercoating solution was prepared so that it would have the compositionshown below. The coating amount of the emulsion is in terms of silver.

The coating solutions for the second layer to the seventh layer wereprepared in the similar manner as that for the first-layer coatingsolution. As a gelatin hardener for each layer,1-oxy-3,5-dichloro-s-triazine sodium salt (H-1), (H-2), and (H-3) wereused. Further, to each layer, were added Ab-1, Ab-2, Ab-3, and Ab-4, sothat the total amounts would be 15.0 mg/m², 60.0 mg/m², 5.0 mg/m², and10.0 mg/m², respectively.

R₁ R₂ a —CH₃ —NHCH₃ b —CH₃ —NH₂ c —H —NH₂ d —H —NHCH₃A mixture in 1:1:1:1 (molar ratio) of a, b, c, and d

Further, to the second layer, the fourth layer, the sixth layer, and theseventh layer, was added 1-(3-methylureidophenyl)-5-mercaptotetrazole inamounts of 0.2 mg/m², 0.2 mg/m², 0.6 mg/m², and 0.1 mg/m², respectively.

Further, to the blue-sensitive emulsion layer and the green-sensitiveemulsion layer, was added 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene inamounts of 1×10⁻⁴ mol and 2×10⁻⁴ mol, respectively, per mol of thesilver halide.

Further, to the red-sensitive emulsion layer, was added a copolymerlatex of methacrylic acid and butyl:acrylate (1:1 in mass ratio; averagemolecular weight, 200,000 to 400,000) in an amount of 0.05 g/m².

Disodium salt of catecol-3,5-disulfonic acid was added to the secondlayer, the fourth layer and the sixth layer so that coating amountswould be 6 mg/m², 6 mg/m² and 18 mg/m², respectively.

Further, in order to prevent irradiation, the following dyes (coatingamounts are shown in parentheses) were added.

(Layer Constitution)

The composition of each layer is shown below. The numbers show coatingamounts (g/m²). In the case of the silver halide emulsion, the coatingamount is in terms of silver.

Support

Polyethylene Resin-Laminated Paper

-   -   (The polyethylene resin on the first layer side contained a        white pigment (TiO₂; content of 16 mass %, ZnO; content of 4        mass %), a fluorescent whitening agent        (4,4′-bis(5-methylbenzoxazolyl)stilbene; content of 0.03 mass %)        and a bluish dye (ultramarine; content of 0.33 mass %). The        amount of the polyethylene resin was 29.2 g/m²)

First Layer (Blue-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion A (gold-sulfur 0.24 sensitized cubes, a 3:7 mixture of thelarge-size emulsion A-1 and the small-size emulsion A-2 (in terms of molof silver)) Gelatin 1.25 Yellow coupler (ExY) 0.57 Color-imagestabilizer (Cpd-1) 0.07 Color-image stabilizer (Cpd-2) 0.04 Color-imagestabilizer (Cpd-3) 0.07 Color-image stabilizer (Cpd-8) 0.02 Solvent(Solv-1) 0.21

Second Layer (Color-Mixing Inhibiting Layer) Gelatin 1.15 Color-mixinginhibitor (Cpd-4) 0.10 Color-image stabilizer (Cpd-5) 0.018 Color-imagestabilizer (Cpd-6) 0.13 Color-image stabilizer (Cpd-7) 0.07 Solvent(Solv-1) 0.04 Solvent (Solv-2) 0.12 Solvent (Solv-5) 0.11

Third Layer (Green-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion C 0.14 (gold-sulfur sensitized cubes, a 1:3 mixture of thelarge-size emulsion C-1 and the small-size emulsion C-2 (in terms of molof silver)) Gelatin 1.21 Magenta coupler (ExM) 0.15 Ultravioletabsorbing agent (UV-A) 0.14 Color-image stabilizer (Cpd-2) 0.003Color-mixing inhibitor (Cpd-4) 0.002 Color-image stabilizer (Cpd-6) 0.09Color-image stabilizer (Cpd-8) 0.02 Color-image stabilizer (Cpd-9) 0.01Color-image stabilizer (Cpd-10) 0.01 Color-image stabilizer (Cpd-11)0.0001 Solvent (Solv-3) 0.09 Solvent (Solv-4) 0.18 Solvent (Solv-5) 0.17

Fourth Layer (Color-Mixing Inhibiting Layer) Gelatin 0.68 Color-mixinginhibitor (Cpd-4) 0.06 Color-image stabilizer (Cpd-5) 0.011 Color-imagestabilizer (Cpd-6) 0.08 Color-image stabilizer (Cpd-7) 0.04 Solvent(Solv-1) 0.02 Solvent (Solv-2) 0.07 Solvent (Solv-5) 0.065

Fifth Layer (Red-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion E 0.16 (gold-sulfur sensitized cubes, a 5:5 mixture of thelarge-size emulsion E-1 and the small-size emulsion E-2 (in terms of molof silver)) Gelatin 0.95 Cyan coupler (ExC-1) 0.023 Cyan coupler (ExC-2)0.05 Cyan coupler (ExC-3) 0.17 Ultraviolet absorbing agent (UV-A) 0.055Color-image stabilizer (Cpd-1) 0.22 Color-image stabilizer (Cpd-7) 0.003Color-image stabilizer (Cpd-9) 0.01 Color-image stabilizer (Cpd-12) 0.01Solvent (Solv-8) 0.05

Sixth Layer (Ultraviolet Absorbing Layer) Gelatin 0.46 Ultravioletabsorbing agent (UV-B) 0.35 Compound (S1-4) 0.0015 Solvent (Solv-7) 0.18

Seventh Layer (Protective Layer) Gelatin 1.00 Acryl-modified copolymerof polyvinyl alcohol 0.4 (modification degree: 17%) Liquid paraffin 0.02Surface-active agent (Cpd-13) 0.02 (ExY)Yellow coupler

(ExY may be called as a comparative coupler Y1.) (ExM) Magenta coupler Amixture in 40:40:40 (molar ratio of

(ExC-1) Cyan coupler

(ExC-2) Cyan coupler

(ExC-3) Cyan coupler

(Cpd-1) Color-image stabilizer

(Cpd-2) Color-image stabilizer

(Cpd-3) Color-image stabilizer

(Cpd-4) Color-mixing inhibitor

(Cpd-5) Color-image stabilizer

(Cpd-6) Color-image stabilizer

(Cpd-7) Color-image stabilizer

(Cpd-8) Color-image stabilizer

(Cpd-9) Color-image stabilizer

(Cpd-10) Color-image stabilizer

(Cpd-11)

(Cpd-12)

(Cpd-13) Surface-active agent A mixture in 7:3 (molar ratio) of

(Cpd-14)

(Cpd-15)

(Cpd-16)

(Cpd-17)

(Cpd-18)

(Cpd-19) Color-mixing inhibitor

(Cpd-20)

(Solv-1)

(Solv-2)

(Solv-3)

(Solv-4)

(Solv-5)

(Solv-7)

(Solv-8)

(Solv-9)

(S1-4)

(UV-1) Ultraviolet absorbing agent

(UV-2) Ultraviolet absorbing agent

(UV-3) Ultraviolet absorbing agent

(UV-5) Ultraviolet absorbing agent

(UV-6) Ultraviolet absorbing agent

(UV-7) Ultraviolet absorbing agent

UV-A: A mixture of UV-1/UV-2/UV-3 = 7/2/2 (mass ratio) UV-B: A mixtureof UV-1/UV-2/UV-3/UV-5/UV-6 = 13/3/3/5/3 (mass ratio) UV-C: A mixture ofUV-1/UV-3 = 9/1 (mass ratio)

Samples P102 to P105 were prepared in the same manner as for Sample P101prepared as described above except that the composition of the firstlayer was changed as described below.

First Layer of Sample P102 (Blue-Sensitive Emulsion Layer) Silverchloroidobromide emulsion A (gold-sulfur 0.24 sensitized cubes, a 3:7mixture of the large-size emulsion A-1 and the small-size emulsion A-2(in terms of mol of silver)) Gelatin 1.25 Yellow coupler (ExY) 0.57Color-image stabilizer (Cpd-2) 0.06 Color-image stabilizer (Cpd-8) 0.07Color-image stabilizer (Cpd-20) 0.11 Solvent (Solv-9) 0.36

First Layer of Sample P103 (Blue-Sensitive Emulsion Layer) Silverchloroidobromide emulsion A (gold-sulfur 0.15 sensitized cubes, a 3:7mixture of the large-size emulsion A-1 and the small-size emulsion A-2(in terms of mol of silver)) Gelatin 1.25 Yellow coupler (Exemplifiedcompound (3)) 0.30 Color-image stabilizer (Cpd-2) 0.06 Color-imagestabilizer (Cpd-8) 0.07 Color-image stabilizer (Cpd-20) 0.11 Solvent(Solv-9) 0.36

In Samples P104 and P105, the yellow coupler in Sample P103 was changedto the yellow couplers shown in Table 10, respectively, in an equivalentmole.

Sample P103 mentioned above as a photosensitive material was processedinto a form of a roll with a width of 127 mm, and the photosensitivematerial was imagewise exposed from a negative film of average density,by using Mini Labo Printer Processor PP350 (trade name) manufactured byFuji Photo Film Co., Ltd. and continuous processing (running test) wasperformed until the volume of the color developer replenisher used inthe following processing step became double the volume of the colordeveloper tank. The photosensitive material was evaluated by subjectingto the following two steps different from each other in the liquidcondition and processing time.

Processing Step A

The processing using the following running processing solution was namedProcessing A. Replenishment Processing step Temperature Time rate* Color38.5° C. 45 sec 45 ml development Bleach-fixing 38.0° C. 45 sec 35 mlRinse (1) 38.0° C. 20 sec — Rinse (2) 38.0° C. 20 sec — Rinse (3)**38.0° C. 20 sec — Rinse (4)** 38.0° C. 20 sec 121 ml  Drying   80° C.(Notes)*Replenishment rate per m² of the light-sensitive material to beprocessed.**A rinse cleaning system RC50D, trade name, manufactured by Fuji PhotoFilm Co. Ltd., was installed in the rinse (3), and the rinse solutionwas taken out from the rinse (3) and sent to a reverse osmosis membranemodule (RC50D) by using a pump. The permeated water obtained in thattank was supplied to the rinse (4), and the concentrated liquid wasreturned to the rinse (3). Pump pressure was controlled such that thewater to be permeated in the reverse osmosis module would be maintained# in an amount of 50 to 300 ml/min, and the rinse solution wascirculated under controlled temperature for 10 hours a day. The rinsewas made in a tank counter-current system from (1) to (4).

The composition of each processing solution was as follows. (Colordeveloper) (Tank solution) (Replenisher) Water 800 ml 800 ml Fluorescentwhitening agent (FL-1) 2.2 g 5.1 g Fluorescent whitening agent (FL-2)0.35 g 1.75 g Triisopropanolamine 8.8 g 8.8 g Polyethyleneglycol 10.0 g10.0 g (Average molecular weight 300) Ethylenediamine tetraacetic acid4.0 g 4.0 g Sodium sulfite 0.10 g 0.20 g Potassium chloride 10.0 g —Sodium 4,5-dihydroxybenzene- 0.50 g 0.50 g 1,3-disulfonateDisodium-N,N-bis(sulfonatoethyl) 8.5 g 14.0 g hydroxylamine4-amino-3-methyl-N-ethyl-N- 4.8 g 14.0 g(β-methanesulfonamidoethyl)aniline •3/2 sulfate•monohydrate Potassiumcarbonate 26.3 g 26.3 g Water to make 1000 ml 1000 ml pH (25° C.,adjusted using sulfuric acid 10.15 and potassium hydroxide)

(Tank (Bleach-fixing solution) solution) (Replenisher) Water 800 ml 800ml Ammonium thiosulfate (750 g/ml) 107 ml 214 mlm-Carboxymethylbenzenesulfinic 8.3 g 16.5 g acid Ammonium iron (III)ethylenediamine 47.0 g 94.0 g tetraacetic acidEthylenediaminetetraacetate 1.4 g 2.8 g Nitric acid (67%) 16.5 g 33.0 gImidazole 14.6 g 29.2 g Ammonium sulfite 16.0 g 32.0 g Potassiummetabisulfite 23.1 g 46.2 g Water to make 1000 ml 1000 ml pH (25° C.,adjusted using nitric 6.5 6.5 acid and aqueous ammonia)

(Rinse solution) (Tank solution) (Replenisher) Sodiumchlorinated-isocyanurate 0.02 g 0.02 g Deionized water 1000 ml 1000 ml(conductivity: 5 μS/cm or less) pH (25° C.) 6.5 6.5Processing step B

Sample P103 was processed into a form of a roll with a width of 127 mm,and the photosensitive material was imagewise exposed from a negativefilm of average density, by using a laboratory processor obtained bymodifying Mini Labo Printer Processor PP350 (trade name) manufactured byFuji Photo Film Co., Ltd. so that the processing time and processingtemperature could be changed, and continuous processing (running test)was performed until the volume of the color developer replenisher usedin the following processing step became double the volume of the colordeveloper tank. The processing using this running processing solutionwas named processing B. Replenishment Processing step Temperature Timerate* Color development 45.0° C. 20 sec  45 ml Bleach-fixing 40.0° C. 20sec  35 ml Rinse (1) 40.0° C. 8 sec — Rinse (2) 40.0° C. 8 sec — Rinse(3)** 40.0° C. 8 sec — Rinse (4)** 38.0° C. 8 sec 121 ml  Drying   80°C. 15 sec (Notes)*Replenishment rate per m² of the light-sensitive material to beprocessed.**A rinse cleaning system RC50D, trade name, manufactured by Fuji PhotoFilm Co., Ltd., was installed in the rinse (3), and the rinse solutionwas taken out from the rinse (3) and sent to a reverse osmosis membranemodule (RC50D) by using a pump. The permeated water obtained in thattank was supplied to the rinse (4), and the concentrated water wasreturned to the rinse (3). Pump pressure was controlled such that thewater to be permeated in the reverse osmosis module would# be maintained in an amount of 50 to 300 ml/min, and the rinse solutionwas circulated under controlled temperature for 10 hours a day. Therinse was made in a tank counter-current system from (1) to (4).

The composition of each processing solution was as follows. (Tank (Colordeveloper) solution) (Replenisher) Water 800 ml 800 ml Fluorescentwhitening agent (FL-3) 4.0 g 8.0 g Residual color reducing agent 3.0 g5.5 g (SR-1) Triisopropanolamine 8.8 g 8.8 g Sodium p-toluenesulfonate10.0 g 10.0 g Ethylenediamine tetraacetic acid 4.0 g 4.0 g Sodiumsulfite 0.10 g 0.10 g Potassium chloride 10.0 g — Sodium4,5-dihydroxybenzene- 0.50 g 0.50 g 1,3-disulfonateDisodium-N,N-bis(sulfonatoethyl) 8.5 g 14.0 g hydroxylamine4-amino-3-methyl-N-ethyl-N- 7.0 g 19.0 g(β-methanesulfonamidoethyl)aniline• 3/2 sulfate•monohydrate Potassiumcarbonate 26.3 g 26.3 g Water to make 1000 ml 1000 ml pH (25° C.,adjusted using sulfuric 10.25 12.6 acid and potassium hydroxide)

(Bleach-fixing solution) (Tank solution) (Replenisher) Water 800 ml 800ml Ammonium thiosulfate (750 g/l) 107 ml 214 ml Succinic acid 29.5 g59.0 g Ammonium iron (III) 47.0 g 94.0 g ethylenediaminetetraacetateEthylenediaminetetraacetic acid 1.4 g 2.8 g Nitric acid (67%) 17.5 g35.0 g Imidazole 14.6 g 29.2 g Ammonium sulfite 16.0 g 32.0 g Potassiummetabisulfite 23.1 g 46.2 g Water to make 1000 ml 1000 ml pH (25° C.,adjusted using nitric 6.00 6.00 acid and aqueous ammonia)

(Rinse solution) (Tank solution) (Replenisher) Sodiumchlorinated-isocyanurate 0.02 g 0.02 g Deionized water 1000 ml 1000 ml(conductivity: 5 μS/cm or less) pH (25° C.) 6.5 6.5Processing Step C

The processing using the running processing solution of Processing B andchanging the carrier-speed of the processor to 1.8 times therebyreducing processing time was named Processing C.

Utilized compounds are shown as follows.

Samples P101 to P105 were evaluated on the following after they werestored under the conditions of 25° C. and a relative humidity of 55%after the coating of the photosensitive material for 10 days.

(Evaluation 1 Rapid Processing Suitability (Dmax Processing Variation))

Each sample was exposed to blue-separated exposure through a 465-nm bandpass filter and an optical wedge for an exposure time of 1/10,000 secondby using a sensitometer. Each sample after the exposure was processedunder the three kinds of processing conditions described below, and themaximum density of the yellow color-formed portion was measured andrapid processing suitability and processing stability were evaluated.Relative values (%) of the maximum density of the yellow color-formedportions in the processing steps B and C relative to the maximum densityof the yellow color-formed portions in the processing step A, werecalculated, respectively.

(Evaluation 2 Calculation of Dmax(UV)/Dmin(UV))

A sample subjected to exposure to white light at a color temperature of4,800° K through a sharp cut filter SC-39 (trade name, manufactured byFuji Photo Film Co., Ltd.) for an exposure time of 1 second at aquantity of exposure light of 2,000 CMS and a nonexposed sample wereeach subjected to the color development processing A as described above.These two samples, exposed and nonexposed, were measured of colordensity. Of the values obtained, the one measured for the sample havinghigher color density (in this Example, the exposed sample) was definedas Dmax, and the one measured for the sample having a lower colordensity (in this Example, the nonexposed sample) was defined as Dmin.Each of the samples after the processing was measured of UV density inthe same manner as in Example 1-1.

Definition of Dmax(UV)/Dmin(UV): This is defined by “the smallest valuein a range of wavelength UV, in which TV is a wavelength within therange of 340 nm or more and 450 nm or less, among values represented by(an absorbance at a wavelength UV, for a portion having the yellowmaximum color density)/(an absorbance at the wavelength UV, for aportion having the yellow minimum color density).”

(Evaluation 3 Calculation of (B−C)/A)

By using the samples as used in Evaluation 2, the yellow density B atthe portion showing the maximum color density (Dmax) (that is, in thisExample, of the exposed sample), and the yellow density C at the portionshowing the minimum color density (Dmin) (that is, in this Example, ofthe nonexposed sample) were measured by use of an HPD densitometer(trade name, manufactured by Fuji Photo Film Co., Ltd., 436 nm). (B−C)/Awas determined by calculation by using the coating amount of thecompound represented by the formula (I), A mol/m².

The results of Evaluations 1, 2 and 3 are shown in Table 10. TABLE 10Rapid processing suitability (Dmax processing Dmax(UV)/ variation) No.Coupler Dmin(UV) (B − C)/A Processing B Processing C P101 ExY 1.26 — 9580 P102 ExY 1.26 — 96 82 P103 (3) 0.74 5250 102 100 P104 (2) 0.77 5050100 99 P105 (4) 0.82 5100 101 99

According to Table 10, it is revealed that use of the photosensitivematerial of the present invention containing the yellow coupler of theformula (I) remarkably decreased fluctuation in the maximum density atthe time of rapid processing.

Example 1-6

Samples P201 to P210 were prepared in the same manner as for Sample P101in Example 1-5 except that the composition of the first layer only waschanged as described below.

First Layer of Sample P201 (Blue-Sensitive Emulsion Layer) Silverchloride emulsion A (a 3:7 mixture (by silver 0.20 molar ratio) ofgold-sulfur-sensitized cube, large-size emulsion A-1 and small sizeemulsion A-2) Gelatin 1.25 Yellow coupler (Exemplified compound 3) 0.15Yellow coupler (ExY) 0.28 Color image stabilizer (Cpd-2) 0.06 Colorimage stabilizer (Cpd-3) 0.07 Color image stabilizer (Cpd-20) 0.11Solvent (Solv-9) 0.36

First Layer of Sample P202 (Blue Sensitive Emulsion Layer) Silverchloride emulsion A (a 3:7 mixture (by silver 0.22 molar ratio) ofgold-sulfur-sensitized cube, large-size emulsion A-1 and small sizeemulsion A-2) Gelatin 1.25 Yellow coupler (Exemplified compound 3) 0.08Yellow coupler (ExY) 0.42 Color image stabilizer (Cpd-2) 0.06 Colorimage stabilizer (Cpd-3) 0.07 Color image stabilizer (Cpd-20) 0.11Solvent (Solv-9) 0.36

In Samples P203 to P210, the yellow coupler in Sample P103 was changedto the yellow couplers shown in Table 11, respectively, in an equivalentmole.

By using Samples P101 to P105 in Example 1-5 and samples P201 to P210described above and after storing the photosensitive material under theconditions of 25° C. and a relative humidity of 55% after the coatingfor 10 days, they were each processed into a roll of a width of 12.7cm×200 m. Then, Evaluations 2 and 3 were performed according to Example1-5, and further Evaluation 4 below was performed.

(Evaluation 4 Static-Induced Fog)

Each roll was rewound at a rate of 100 m/minute in an atmosphere of 10°C. and a relative humidity of 25% in the absence of light and theabove-mentioned processing step B was performed without exposure tolight. The number of static-induced fogs that occurred in the whitebackground after the processing was visually detected. Relative values(%) relative to the number of static-induced fogs occurring in SampleP101 are shown in Table 11 below. TABLE 11 Static- No. CouplerDmax(UV)/Dmin(UV) (B − C)/A induced fog P101 ExY 1.26 — 100 P102 ExY1.26 — 120 P103  (3) 0.74 5250 30 P104  (2) 0.77 5050 33 P105  (4) 0.825100 38 P201 ExY/(3) *1 0.93 10000 48 P202 ExY/(3) *2 1.05 20000 63 P203(21) 0.83 4620 38 P204 (22) 0.83 4600 39 P205 (23) 0.82 4700 37 P206(24) 0.75 5080 32 P207 (25) 0.77 5050 33 P208 (26) 0.75 5100 32 P209(27) 0.77 5000 32 P210 (3)/(27) *3 0.75 5150 31*1 Mixture of 50:50 (molar ratio)*2 Mixture of 75:25 (molar ratio)*3 Mixture of 50:50 (molar ratio)

According to Table 11, it is revealed that use of the light-sensitivematerial of this invention results in a remarkably decreased occurrenceof static-induced fog.

Example 1-7

In the Examples 1-5 and 1-6, the composition of the fifth layer wasaltered as shown below to prepare a sample.

The sample was evaluated according to the method used in Examples 1-5and 1-6, with the result that the samples according to the presentinvention were excellent in rapid processability (rapid processingsuitability), and resistance to static-induced fog.

Fifth Layer (Red-Sensitive Emulsion Layer) Silver chlorobromide emulsionE 0.10 (gold-sulfur sensitized cubes, a 5:5 mixture of the large-sizeemulsion E-1 and the small-size emulsion E-2 (in terms of mol ofsilver)) Gelatin 1.11 Cyan coupler (ExC-1) 0.02 Cyan coupler (ExC-3)0.01 Cyan coupler (ExC-4) 0.11 Cyan coupler (ExC-5) 0.01 Color-imagestabilizer (Cpd-1) 0.01 Color-image stabilizer (Cpd-6) 0.06 Color-imagestabilizer (Cpd-7) 0.02 Color-image stabilizer (Cpd-9) 0.04 Color-imagestabilizer (Cpd-10) 0.01 Color-image stabilizer (Cpd-14) 0.01Color-image stabilizer (Cpd-15) 0.12 Color-image stabilizer (Cpd-16)0.01 Color-image stabilizer (Cpd-17) 0.01 Color-image stabilizer(Cpd-18) 0.07 Color-image stabilizer (Cpd-20) 0.01 Ultraviolet absorbingagent (UV-7) 0.01 Solvent (Solv-5) 0.1  (ExC-4) Cyan coupler

(ExC-5) Cyan coupler

Example 2-1

Sample 2-001 was prepared in the same manner as in Sample P101 ofExample 1-5, except that for the sample P101 produced in the aboveExample 1-5, in the third layer, the amount to be used (coating amount)of the solvent (Solv-5) was changed into 0.10 g/m² and 0.07 g/m² of thefollowing solvent (Solv-6) was used, in the seventh layer, thesurfactant (Cpd-13) was replaced by the following compounds and thefollowing compounds were used as the ultraviolet absorbers UV-A andUV-B. As shown above, in the thus-prepared Sample 2-001, the first layerwas changed to any of BL-A to BL-E shown below and the composition ofthe fifth layer was changed to those shown by any of RL-A to RL-K. Thesefirst and fifth layers were combined, as shown in Table 12, to producesamples 2-101 to 2-116.

(Cpd-13) Surface-active agent to be used in Example 2-1

A mixture in 6:2:2 (molar ratio) of

1st layer alteration of the composition of the blue-sensitive emulsionlayer

BL-A: Silver chloroiodobromide emulsion A (gold-sulfur 0.24 sensitizedcubes, a 3:7 mixture of the large-size emulsion A-1 and the small-sizeemulsion A-2 (in terms of mol of silver)) Gelatin 1.20 Yellow coupler(Yellow coupler for comparison Y) 0.53 Color-image stabilizer (Cpd-2)0.06 Color-image stabilizer (Cpd-8) 0.07 Color-image stabilizer (Cpd-14)0.07 Solvent (Solv-9) 0.20

BL-B: Silver chloroiodobromide emulsion A (gold-sulfur 0.15 sensitizedcubes, a 3:7 mixture of the large-size emulsion A-1 and the small-sizeemulsion A-2 (in terms of mol of silver)) Gelatin 0.87 Yellow coupler(Exemplified compound (3)) 0.30 Color-image stabilizer (Cpd-2) 0.06Color-image stabilizer (Cpd-8) 0.07 Color-image stabilizer (Cpd-14) 0.07Solvent (Solv-9) 0.20BL-C:

In BL-B, the yellow coupler was changed to an equal mol of theexemplified compound (67).

BL-D:

In BL-B, the yellow coupler was changed to an equal mol of theexemplified compound (51).

BL-E:

In BL-B, the yellow coupler was changed to an equal mol of theexemplified compound (56).

5th layer alteration of the composition of the red-sensitive emulsionlayer

RL-A: Silver chloroiodobromide emulsion E 0.17 (gold-sulfur sensitizedcubes, a 5:5 mixture of the large-size emulsion E-1 and the small-sizeemulsion E-2 (in terms of mol of silver)) Gelatin 1.30 Cyan coupler(Cyan coupler for comparison C1) 0.30 Color-image stabilizer (Cpd-1)0.01 Color-image stabilizer (Cpd-6) 0.06 Color-image stabilizer (Cpd-7)0.02 Color-image stabilizer (Cpd-9) 0.04 Color-image stabilizer (Cpd-10)0.01 Color-image stabilizer (Cpd-14) 0.01 Color-image stabilizer(Cpd-15) 0.12 Color-image stabilizer (Cpd-16) 0.01 Color-imagestabilizer (Cpd-17) 0.01 Color-image stabilizer (Cpd-18) 0.07Color-image stabilizer (Cpd-20) 0.01 Ultraviolet absorbing agent (UV-7)0.01 Solvent (Solv-5) 0.15RL-B:

In RL-A, the amount of the silver chlorobromoiodide emulsion E wasaltered to 0.08 g/m² and the cyan coupler was altered to 0.15 g/m² ofthe exemplified compound (CC-50).

RL-C:

In RL-B, the cyan coupler (CC-50) was changed to an equal mol of theexemplified compound (CC-57).

RL-D:

In RL-B, the cyan coupler (CC-50) was changed to an equal mol of theexemplified compound (CC-56).

RL-E:

In RL-B, the cyan coupler (CC-50) was changed to an equal mol of theexemplified compound (CC-47).

RL-F:

In RL-B, the cyan coupler (CC-50) was changed to an equal mol of theexemplified compound (CC-10).

RL-G:

In RL-A, the amount of the silver chlorobromoiodide emulsion E waschanged to 0.10 g/m² and the cyan coupler was changed to 0.10 g/m² ofthe exemplified compound (CC-50), 0.04 g/m of the above-mentioned(EXC-3), and 0.01 g/m² of the below mentioned (ExC-4).

RL-H:

In RL-G, the cyan coupler (CC-50) was changed to an equal mol of theexemplified compound (CC-57).

RL-I:

In RL-G, the cyan coupler (CC-50) was changed to an equal mol of theexemplified compound (CC-56).

RL-J:

In RL-G, the cyan coupler (CC-50) was changed to an equal mol of theexemplified compound (CC-47).

RL-K:

In RL-G, the cyan coupler (CC-50) was changed to an equal mol of theexemplified compound (CC-10).

Coupler for comparison Y1

Coupler for comparison C1

Evaluation was carried out for the photosensitive material 2-113 bysubjecting to the image-wise exposure, the continuous treatment (runningtest) and the two processing steps A and B in the same manner as in theExample 1-5, except that, in the processings A and B of Example 1-5, thephotosensitive material P103 was replaced by the above-mentionedphotosensitive material 2-113 and color-developing time in theprocessing B was changed into 17 seconds.

The coating solutions for forming photographic constituent layers werecoated and thus Samples (light-sensitive materials) 2-101 to 2-116 wereprepared. These light-sensitive materials were used as samples. Thesesamples were stored for 10 days under the conditions of 25° C. and 55%RH. After that, these samples were subjected to the followingevaluations.

(Evaluation 1 Color Reproductively)

The samples were subjected to 3-color separation exposure and thesamples after the exposure underwent color development processingaccording to the process A. In this way, monochromatic samples, i.e.,yellow, magenta, and cyan samples, were obtained.

As the light source, a semiconductor laser was used to obtain a lightsource at 688 nm (R light), a semiconductor laser was combined with SHGto obtain a light source at 532 nm (G light) and a light source at 473nm (B light). The quantity of R light was modulated with using an outermodulator, and scanning exposure was performed to a sample moving in adirection orthogonal to the scanning direction, by reflecting the lighton a rotating polygon. The scanning exposure was performed at thedensity of 400 dpi and the average exposure time per 1 pixel was 8×10⁻⁸second. The temperature of the semiconductor laser was kept constant,with using a Peltier element, in order to prevent the change in quantityof light due to change in temperature.

By using the samples thus obtained, the volume of Lab space, which canbe reproduced in accordance with the method described inJP-A-2001-194755 (paragraph Nos. 0014-0019 and Example 1), was computed.At Dmax=2.2 under a light source of D50, the volumes of space of L* of50 or more of the samples, as relative values (percentages) on the basisof Sample 2-101, were computed.

(Evaluation 2 Processing Stability at the Time of Rapid Processing)

By using the light source (apparatus) for exposure of the evaluation 1,the exposing condition of the samples was determined such that a graygradation was given in the process A. After being given the exposure,the samples were processed for development in the process B at a1.2-fold transfer speed. The density at the process B of the exposedregion, which gave a density of 2.0 at the process A, was measured andthe density differences of yellow and cyan ((ΔB, ΔR) of the process Bwith respect to process A were computed.

(Evaluation 3, Desilverization)

Each sample was exposed to white light having a color temperature of4800 degrees at 500 CMS. The exposed sample was treated in theprocessing solution used in the process step B wherein the bleaching andfixing time is shortened to 12 seconds. The amount of the residualsilver of the treated sample was measured quantitatively by using afluorescent X-rays.

(Evaluation 4, Residual Color)

Each sample was treated in the process step B in an unexposed statewherein the carrying speed was increased 1.4 times.

As to the treated sample, the density of yellow was measured in Status Aby using an X-rite 310 Densitometer (manufactured by X-rite Company).The density of each sample was again measured after additionally washedusing excess of ion exchanged water at 40° C. for 5 minutes. A change ΔYin yellow density between the samples before and after washedadditionally with water was calculated to evaluate the degree ofresidual color.

Samples 2-112 to 2-116 were used together with the following cyancoupler ExC-4 as in the fifth layer.

The evaluations results are shown in Table 12. TABLE 12 Processingstability Color at the time of rapid Desilverizing Residual ConstitutionCoupler in Constitution Coupler in reproductivity processing abilitycolor No. of first layer first layer of fifth layer fifth layer(Relative %) ΔB ΔR (g/m²) ΔY 2-101 BL-A Coupler for RL-A Coupler for100.0 −0.12 −0.10 0.07 0.051 comparison comparison Y1 C1 2-102 BL-ACoupler for RL-B CC-50 104.5 −0.09 −0.03 0.04 0.041 comparison Y1 2-103BL-B (3) RL-A Coupler for 104.5 −0.06 −0.10 0.04 0.035 comparison C12-104 BL-B (3) RL-B CC-50 111.0 −0.03 −0.02 0.01 0.005 2-105 BL-B (3)RL-C CC-57 111.0 −0.03 −0.02 0.01 0.005 2-106 BL-B (3) RL-D CC-56 111.0−0.03 −0.02 0.01 0.005 2-107 BL-B (3) RL-E CC-47 110.0 −0.03 −0.03 0.010.005 2-108 BL-B (3) RL-F CC-10 110.0 −0.03 −0.02 0.01 0.008 2-109 BL-C(67)  RL-C CC-57 111.0 −0.03 −0.02 0.01 0.005 2-110 BL-D (51)  RL-CCC-57 111.0 −0.03 −0.02 0.01 0.005 2-111 BL-E (56)  RL-C CC-57 110.5−0.03 −0.02 0.01 0.005 2-112 BL-B (3) RL-G CC-50/EXC-3/EXC-4 109.5 −0.03−0.03 0.01 0.012 2-113 BL-C (67)  RL-H CC-57/EXC-3/EXC-4 109.5 −0.03−0.02 0.01 0.010 2-114 BL-D (51)  RL-I CC-56/EXC-3/EXC-4 109.5 −0.03−0.02 0.01 0.010 2-115 BL-E (56)  RL-J CC-47/EXC-3/EXC-4 109.0 −0.03−0.04 0.01 0.011 2-116 BL-D (51)  RL-K CC-10/EXC-3/EXC-4 109.0 −0.03−0.04 0.01 0.011

It can be found from the results shown in Table 12 that the use of acombination of the yellow coupler used in the present invention and thecyan coupler used in the present invention ensured the silver halidephotographic light-sensitive material which was excellent in colorreproducibility, and in all of desilverizing ability, residual color andstability during rapid processing.

Example 2-2

The positions of the first and fifth layers in the samples 2-101 to2-116 in Example 2-1 were reversed to produce samples 2-201 to 2-216.These samples 2-201 to 2-216 were evaluated according to the method usedin Example 2-1. As a result, an improvement in yellow and magenta colordensity was found in a gray process when using the sample using,particularly, the cyan coupler to be used in the present invention.Also, the results of the evaluations 1 to 4, similar to Example 2-1,showed that the use of a combination of the yellow coupler used in thepresent invention and the cyan coupler used in the present inventionensured the silver halide photographic light-sensitive material whichwas excellent in color reproducibility, and in all of desilverizingability, residual color and stability during rapid processing.

Example 2-3

The magenta coupler contained in the third layer of each sample ofExamples 2-1 and 2-2 was changed as shown below to produce samples. Eachresulting sample was evaluated according to the methods used in Examples2-1 and 2-2. As a result, it was found that a silver halide colorphotographic light-sensitive material having excellent colorreproducibility and rapid processability was obtained according to thepresent invention.

3rd Layer Modification of the Composition of the Green-SensitiveEmulsion Layer

GL-A:

The magenta coupler in the third layer in Example 2-1 was altered to 1.5equivalent mol of the magenta coupler M1.

GL-B:

The magenta coupler in the third layer in Example 2-1 was altered to 1.5equivalent mol of the magenta coupler M2.

Example 2-4

In Example 2-1, the silver halide emulsion was altered as shown below toprepare a sample, which was evaluated according to the method used inExample 2-1. As a result, it was found that according to the presentinvention, a silver halide color photographic light-sensitive materialhaving excellent color reproducibility and rapid processability wasobtained.

First layer: Mixture of (Emulsion B-H) and (Emulsion B-L) in a ratio of4:6 (in silver molar ratio)

Third layer: Mixture of (Emulsion G-H) and (Emulsion G-L) in a ratio of5:5 (in silver molar ratio)

Fifth layer: Mixture of (Emulsion R-H) and (Emulsion R-L) in a ratio of6:4 (in silver molar ratio)

(Preparation of Emulsion B-H)

A cubic high-silver chloride content emulsion which had a sphereequivalent diameter grains of 0.55 μm and a coefficient of variation of10% was prepared by a usual method in which silver nitrate and sodiumchloride were added simultaneously to an aqueous gelatin solution whichwas stirred to mix them. Potassium bromide (KBr) and K₄-[Ru(CN)₆] wereadded to the reaction solution at the step of the addition of from 80%to 90% of the entire silver nitrate amount used in emulsion grainformation, so that the KBr amount became 3 mole % per mole of thefinished silver halide. When the addition of 90% of the entire silvernitrate amount was completed, an aqueous solution of potassium iodide(KI) was added, so that the KI amount became 0.3 mole % per mole of thefinished silver halide. K₂-[Ir(5-methylthiazole)Cl₅] and K₂-[Ir(H₂O)Cl₅]were added to the reaction solution at the step of the addition of from92% to 98% of the entire silver nitrate amount used in emulsion grainformation. The resulting emulsion was subjected to desalting treatmentand then a gelatin was added to the emulsion to redisperse. To theemulsion were added sodium thiosulfonate and the following sensitizingdyes A and B, and the resulting emulsion was optimally ripened withsodium thiosulfate pentahydrate as a sulfur sensitizer andbis(1,4,5-trimethyl-1,2,4-triazolium-3-thiolate)aurate(I)tetrafluoroborate as a gold sensitizer. Further,1-phenyl-5-mercaptotetrazole and1-(5-methylureidophenyl)-5-mercaptotetrazole were added to theresultant, thereby Emulsion B-H being prepared.

(Preparation of Emulsion B-L)

A cubic high-silver chloride content emulsion which had a sphereequivalent diameter of grains of 0.45 μm and a coefficient of variationof 10%, was prepared in the same manner as in the production of theemulsion B-H, except that the rate of the addition of silver nitrate andsodium chloride was changed. The resulting emulsion was named as anemulsion B-L.

(Preparation of Emulsion G-H)

A cubic high-silver chloride content emulsion which had a sphereequivalent diameter of grains of 0.35 μm and a coefficient of variationof 10% was prepared by a usual method in which silver nitrate and sodiumchloride were added simultaneously to an aqueous gelatin solution whichwas stirred, to mix them. K₄-[Ru(CN)₆] was added to the reactionsolution at the step of the addition of from 80% to 90% of the entiresilver nitrate amount used in emulsion grain formation. Potassiumbromide (KBr) was added to the reaction solution at the step of theaddition of from 80% to 100% of the entire silver nitrate amount used inemulsion grain formation, so that the KBr amount became 4 mole % permole of the finished silver halide. When the addition of 90% of theentire silver nitrate amount was completed, an aqueous solution ofpotassium iodide (KI) was added, so that the KI amount became 0.2 mole %per mole of the finished silver halide. K₂-[Ir(5-methylthiazole)Cl₅] wasadded to the reaction solution at the step of the addition of from 92%to 95% of the entire silver nitrate amount used in emulsion grainformation. Further, K₂-[Ir(H₂O)Cl₅] was added to the reaction solutionat the step of the addition of from 92% to 98% of the entire silvernitrate amount used in emulsion grain formation. The resulting emulsionwas subjected to desalting treatment and then a gelatin was added to theemulsion to redisperse. To the emulsion was added sodium thiosulfonateand the resultant emulsion was optimally ripened with sodium thiosulfatepentahydrate as a sulfur sensitizer andbis(1,4,5-trimethyl-1,2,4-triazolium-3-thiolate)aurate(I)tetrafluoroborate as a gold sensitizer. Further, the followingsensitizing dye D, 1-phenyl-5-mercaptotetrazole,1-(5-methylureidophenyl)-5-mercaptotetrazole and potassium bromide wereadded to the resultant, thereby Emulsion G-H being prepared.

(Preparation of Emulsion G-L)

A cubic high-silver chloride content emulsion which had a sphereequivalent diameter of grains of 0.28 μm and a coefficient of variationof 10% was prepared in the same manner as in the production of theemulsion G-H, except that the rate of the addition of silver nitrate andsodium chloride was changed. The resulting emulsion was named as anemulsion G-L.

(Preparation of Emulsion R-H)

A cubic high-silver chloride content emulsion which had a sphereequivalent diameter of grains of 0.35 μm and a coefficient of variationof 10% was prepared by a usual method in which silver nitrate and sodiumchloride were added simultaneously to an aqueous gelatin solution whichwas stirred. K₄[Ru(CN)₆] was added to the reaction solution at the stepof the addition of from 80% to 90% of the entire silver nitrate amountused in emulsion grain formation. Potassium bromide (KBr) was added tothe reaction solution at the step of the addition of from 80% to 100% ofthe entire silver nitrate amount used in emulsion grain formation, sothat the KBr amount became 4.3 mole % per mole of the finished silverhalide. When the addition of 90% of the entire silver nitrate amount wascompleted, an aqueous solution of potassium iodide (KI) was added, sothat the KI amount became 0.15 mole % per mole of the finished silverhalide. K₂[Ir(5-methylthiazole)Cl₅] was added to the reaction solutionat the step of the addition of from 92% to 95% of the entire silvernitrate amount used in emulsion grain formation. Further, K₂[Ir(H₂O)Cl₅]was added to the reaction solution at the step of the addition of from92% to 95% of the entire silver nitrate amount used in emulsion grainformation. Further, K₂[Ir(H₂O)Cl₅] was added to the reaction solution atthe step of the addition of from 92% to 98% of the entire silver nitrateamount used in emulsion grain formation. The resulting emulsion wassubjected to desalting treatment and then a gelatin was added to theemulsion to redisperse. To the emulsion was added sodium thiosulfonateand resultant emulsion was optimally ripened with sodium thiosulfatepentahydrate as a sulfur sensitizer andbis(1,4,5-trimethyl-1,2,4-triazolium-3-thiolate)aurate(I)tetrafluoroborate as a gold sensitizer. Further, the followingsensitizing dye H, 1-phenyl-5-mercaptotetrazole,1-(5-methylureidophenyl)-5-mercaptotetrazole, the following compound Iand potassium bromide were added to the resultant, thereby Emulsion R-Hbeing prepared.

(Preparation of Emulsion R-L)

A cubic high-silver chloride content emulsion which had a sphereequivalent diameter of grains of 0.28 μm and a coefficient of variationof 10% was prepared in the same manner as in the production of theemulsion R-H, except that the rate of the addition of silver nitrate andsodium chloride was changed. The resulting emulsion was named as anemulsion R-L.

Example 2-5

The samples produced in Examples 2-1 to 2-4 were scan-exposed using theapparatus shown below, to evaluate the resulting samples according tothe methods used in Examples 2-1 to 2-4. As a result, it was found thatwhen the sample having the structure of the present invention was used,the effects of the present invention, such as excellent in Colorreproductivity and rapid processability, were exhibited particularlysignificantly.

Digital Minilabo Frontier 330 (trade name, manufactured by Fuji PhotoFilm Co., Ltd.), Lambda 130 (trade name, manufactured by Durst),LIGHTJET 5000 (trade name, manufactured by Gretag).

Example 2-6

The following alterations 1) and 2) were made in the sample 109described in Example 1 of JP-A-2001-142181 to produce a sample.

1) Each composition of the 15th layer, the 16th layer and the 17th layerwas altered as follows.

2) In all of the fourth, fifth and sixth layers of the sample 101 ofExample 1, only 50% of the mol ratio of each of C-1 and C-2 used in thesample was replaced by the exemplified compound CC-50 that can be usedin the present invention. Specifically, C-1 was replaced by a mixture(used in the fourth and fifth layers) of C-1 (the compound described inExample 1 of JP-A-2001-142181) and CC-50 that can be used in the presentinvention, and C-2 was replaced by a mixture (used in the sixth layer)of C-2 (the compound described in Example 1 of JP-A-2001-142181) andCC-50 that can be used in the present invention.

15th Layer (Low Sensitivity Blue-Sensitive Emulsion Layer) Silverbromoiodide emulsion L silver 0.11 Silver bromoiodide emulsion M silver0.15 Gelatin 0.80 Yellow coupler (exemplified compound (62) to be usedin 0.30 the present invention) Compound Cpd-M 0.01 High-boiling pointorganic solvent (tricresyl phosphate) 0.05

16th Layer (Middle Sensitivity Blue-Sensitive Emulsion Layer) Silverbromoiodide emulsion N amount of silver 0.15 Silver bromoiodide emulsionO amount of silver 0.15 Gelatin 0.76 Yellow coupler (exemplifiedcompound (62) to 0.34 be used in the present invention) Compound Cpd-N0.002 High-boiling point organic solvent 0.06 (tricresyl phosphate)

17th Layer (High Sensitivity Blue-Sensitive Emulsion Layer) Silverbromoiodide emulsion O amount of silver 0.15 Silver bromoiodide emulsionP amount of silver 0.15 Gelatin 1.10 Yellow coupler (exemplifiedcompound (62) 0.92 to be used in the present invention) Compound Cpd-N0.005 Compound Cpd-Q 0.20 High-boiling point organic solvent 0.17(tricresyl phosphate)

Silver bromoiodide emulsions L to P and Compounds Cpd-M, N and Q werethe same as those described in Example 1 in JP-A-2001-142181.

Using the sample obtained in this manner, exposure and developmentprocessing (development processing A) were carried out using the methodsdescribed in Example 1 of JP-A-2001-142181, to confirm the effects ofthe present invention.

Example 3-1

Sample 3-001 was prepared in the same manner as in Sample P101 ofExample 1-5, except that for the sample P101 produced in the aboveExample 1-5, in the third layer, the amount to be used (coating amount)of the solvent (Solv-5) was changed into 0.10 g/m² and 0.07 g/m² of thefollowing solvent (Solv-6) was used, in the seventh layer, thesurfactant (Cpd-13) was replaced by the following compounds and thebelow-shown compounds were used as the ultraviolet absorbers UV-A andUV-B. In the thus-prepared Sample 3-001, the first layer was changedinto the following composition, to prepare Sample Nos. 3-101 to 3-130,respectively.

(Cpd-13) Surface-Active Agent to be used in Example 3-1

A mixture in 6:2:2 (molar ratio) of

1st Layer Alteration of the Composition of the Blue-Sensitive EmulsionLayer

Composition of Sample No. 3-101: Silver chlorobromoiodide emulsion A(sulfur-plus-gold 0.24 sensitized cubic grains, a 3:7 (in silver molarratio) mixture composed of the large-size emulsion A-1 and thesmall-size emulsion A-2) Gelatin 1.20 Yellow coupler (comparativecoupler Y1) 0.53 Color image stabilizer (Cpd-2) 0.06 Color imagestabilizer (Cpd-8) 0.07 Color image stabilizer (Cpd-14) 0.07 Solvent(comparative solvent DBP) 0.20

(comparative solvent DBP: dibutyl phthalate)

Composition of Sample No. 3-102:

The solvent of the 1st layer of the sample No. 3-101 was replaced withthe solvent (S-I-6) in the present invention.

Composition of Sample No. 3-103: Silver chlorobromoiodide emulsion A(sulfur-plus-gold 0.15 sensitized cubic grains, a 3:7 (in silver molarratio) mixture composed of the large-size emulsion A-1 and thesmall-size emulsion A-2) Gelatin 0.87 Yellow coupler (Exemplifiedcompound (3)) 0.30 Color image stabilizer (Cpd-2) 0.06 Color imagestabilizer (Cpd-8) 0.07 Color image stabilizer (Cpd-14) 0.07 Solvent(comparative solvent DBP) 0.20Composition of Sample No. 3-104:

The solvent of the 1st layer of the sample No. 3-103 was replaced withthe solvent (S-I-6) in the present invention.

Compositions of Samples Nos. 3-105 to 3-130

The yellow coupler and the solvent of the 1st layer of the sample No.3-104 were replaced according to Table 13. The replacement of thecoupler was made on equimolar basis and the replacement of the solventwas made on the same mass basis.

Evaluation was carried out by subjecting to the image-wise exposure, thecontinuous treatment (running test) and the two processing steps A and Bin the same manner as in the Example 1-5, except that, in theprocessings A and B of Example 1-5, the photosensitive material P103 wasreplaced by the above-mentioned photosensitive material 3-001 andcolor-developing time in the processing B was changed into 17 seconds.

The coating solutions for forming photographic constituent layers werecoated and thus light-sensitive materials were prepared. Theselight-sensitive materials were used as samples. These samples werestored for 10 days under the conditions of 25° C. and 55% RH. Afterthat, these samples were subjected to the following evaluations.

With respect to (Evaluation 1 Color reproductivity) and (Evaluation 2processing stability at the time of rapid processing), tests andevaluations were performed in the same manner as in Example 2-1.

(Evaluation 3 Preservation Stability in an Unexposed State)

Two samples (Control and Aging) stored in different conditions wereprepared from each sample: in one test (Control), the sample aftercoated was stored in the condition of a temperature of 25° C. and arelative humidity of 55% for 10 days and in another test, the sampleafter the above test was further stored in the condition of atemperature of 40° C. and a relative humidity of 75% for 4 days.Thereafter, exposure for separation gradation in which three-coloredseparation was conducted was carried out using the exposure apparatusused in the Evaluation 1 and developing treatment was carried out in theprocess step B to perform sensitometry. The yellow density of the sample(Aging) which had been stored in the condition of a temperature of 40°C. and a relative humidity of 75% and exposed at the intensity giving ayellow density of 1.8 to the sample (Control) which had been stored inthe condition of a temperature of 25° C. and a relative humidity of 55%,was measured. A difference (ΔB Aging) in the density between the Agingsample and the Control sample was calculated.

(Evaluation 4 Fastness Against Humidity and Heat)

The sample for Control produced in the Evaluation 3 was stored at 80° C.under a relative humidity of 70% for 21 days to measure each densitybefore and after the test. The relative residual rate of the yellowcolor developed portion of the sample after stored at the point wherethe initial density was 1.8 was calculated.

(Evaluation 5 Light Fastness)

The sample for Control produced in the Evaluation 3 was used to measureeach density before and after it was stored for 14 days under a Xe-lightsource at an intensity of 100,000 Lux. The relative residual rate of theyellow color developed portion of the sample after stored at the pointwhere the initial density was 1.0 was calculated.

The evaluations results are shown in Table 13. TABLE 13 Fastness againsthumidity Processing stability at the Stability in an and heat Coupler inthe Solvent for the first time of rapid processing unexposed state(Residual No. first layer layer ΔB ΔB Aging rate %) 3-101 Coupler forSolvent for −0.10 −0.11 80 comparison Y1 comparison DBP 3-102 Couplerfor S-I-6 −0.11 −0.03 86 comparison Y1 3-103  (3) Solvent for −0.03−0.10 96 comparison DBP 3-104  (3) S-I-6 −0.03 −0.03 97 3-105 (67)Solvent for −0.03 −0.10 96 comparison DBP 3-106 (67) S-I-6 −0.03 −0.0397 3-107 (51) Solvent for −0.03 −0.10 96 comparison DBP 3-108 (51) S-I-6−0.03 −0.03 97 3-109 (56) Solvent for −0.03 −0.10 97 comparison DBP3-110 (56) S-I-6 −0.03 −0.03 98 3-111 (51) S-I-2 −0.03 −0.02 98 3-112(51) S-I-22 −0.03 −0.02 98 3-113 (51) S-I-6/S-II-7 *1) −0.01 −0.04 973-114 (51) S-I-6/S-II-2 *1) −0.02 −0.04 97 3-115 (51) S-III-3 −0.03−0.02 98 3-116 (51) S-III-6 −0.03 −0.02 98 3-117 (51) S-IV-2 −0.02 −0.0397 3-118 (51) S-V-1 −0.03 −0.01 99 3-119 (51) S-V-7 −0.03 −0.01 99 3-120(51) S-VI-1 −0.03 −0.01 99 3-121 (56) S-I-6/ST-II-121 *2) −0.01 −0.02 983-122 (56) S-I-6/ST-II-122 *2) −0.01 −0.02 98 3-123 (56) S-I-6/ST-III-18*2) 0.00 −0.02 98 3-124 (67) S-I-6/ST-V-25 *2) −0.01 −0.02 98 3-125 (67)S-I-6/ST-IV-5 *2) −0.03 −0.01 98 3-126 (67) S-I-6/ST-IV-72 *2) −0.03−0.01 98 3-127 (67) S-I-6/P2 *3) −0.03 −0.02 98 3-128 (67) S-I-6/P10 *3)−0.04 −0.02 98 3-129 (67) S-I-6/P60 *3) −0.03 −0.02 98 3-130 (67)S-I-6/PP-16 *3) −0.02 −0.02 98*1) Mixture (mass ratio: 1/4)*2) Mixture (mass ratio: 1/3)*3) Mixture (mass ratio: 1/5)

When the yellow coupler according to the present invention and thecompound according to the present invention were used, a silver halidecolor photographic light-sensitive material was obtained which wasexcellent in stability in rapid processing, stability in an unexposedstate and image fastness.

Example 3-2

The coupler and the solvent in the first layer in the samples 3-101 and3-102 of Example 3-1 were altered, as shown in Table 14, to preparesamples 3-201 and 3-202. Similarly, the coupler and the solvent in thefirst layer in the sample 3-104 of Example 3-1 were altered, as shown inTable 14, to prepare samples 3-203 to 3-217. These resulting sampleswere evaluated according to the method used in Example 3-1. As a result,silver halide color photographic light-sensitive materials excellent inrapid processability and color reproducibility were obtained when theyellow coupler according to the present invention and the compoundaccording to the present invention were used in combination. TABLE 14Processing stability at the time Color of rapid reproducibility Couplerin the Solvent for the processing (Relative No. first layer first layerΔB rate %) 3-201 Coupler for Solvent for −0.1 99.0 comparison Y1comparison DBP 3-202 Coupler for S-I-6 −0.11 100.0 comparison Y1 3-203(3) S-I-6 −0.03 106.2 3-204 (3) S-I-1 −0.03 105.8 3-205 (3) S-I-2 −0.03105.6 3-206 (3) S-III-3 −0.01 105.3 3-207 (3) S-IV-7 −0.03 105.6 3-208(3) S-V-1 −0.03 105.3 3-209 (3) ST-I-4 −0.03 106.2 3-210 (3) ST-I-68−0.05 106.5 3-211 (3) S-I-6/ST-I-68 *1) −0.03 106.5 3-212 (3)S-III-3/ST-I-68 *1) −0.03 106.2 3-213 (51)  S-I-2 −0.03 105.0 3-214(51)  S-I-6 −0.03 105.2 3-215 (51)  ST-I-4 −0.03 105.0 3-216 (51) ST-I-68 −0.03 105.8 3-217 (51)  S-I-6/ST-I-68*1) −0.03 105.8*1) Mixture (mass ratio: ⅓)

Example 3-3

In the samples 3-202 and 3-214 of Example 3-2, only the amount of thesolvent was altered, to prepare samples, in which the ratio (the oilsoluble content/Cp ratio) of the total amount of the color-imagestabilizer and solvent to the coupler in the first layer was altered, asshown in Table 15. In this alteration of the composition, the ratio ofthe total mass of the coupler, color stabilizer and solvent to thegelatin in the first layer was made constant. The light fastness of eachof these samples was evaluated, to find that the yellow coupleraccording to the present invention was significantly improved in lightfastness by increasing the amount of the solvent. TABLE 15 Oil solubleCoupler in the content/Cp Light fastness No. first layer ratio (Residualrate %) 3-301 Coupler for 0.75 80 comparison Y1 3-302 Coupler for 1.5 76comparison Y1 3-303 Coupler for 2.0 74 comparison Y1 3-304 Coupler for2.5 73 comparison Y1 3-305 (51) 0.75 75 3-306 (51) 1.5 80 3-307 (51) 2.091 3-308 (51) 2.5 93

Example 3-4

In Example 3-1, the silver halide emulsion was altered as shown below toprepare a sample, which was evaluated according to the method used inExample 3-1. As a result, it was found that according to the presentinvention, a silver halide color photographic light-sensitive materialexcellent in color reproducibility, rapid processability andpreservation stability in the unexposed state of a light-sensitivematerial was obtained.

First layer: Mixture of (Emulsion B-H) and (Emulsion B-L) in a ratio of4:6 (in silver molar ratio)

Third layer: Mixture of (Emulsion G-H) and (Emulsion G-L) in a ratio of5:5 (in silver molar ratio)

Fifth layer: Mixture of (Emulsion R-H) and (Emulsion R-L) in a ratio of6:4 (in silver molar ratio)

In the above, Emulsion B-H, Emulsion B-L, Emulsion G-H, Emulsion G-L,Emulsion R-H and Emulsion R-L each were prepared in the same manner asin Example 2-4 and used as the amount (ratio) of use described above.

Example 3-5

In the Examples 3-1 to 3-4, the composition of the fifth layer wasaltered as shown below to prepare a sample. The sample was evaluatedaccording to the method used in Examples 3-1 to 3-4, with the resultthat according to the structure of the present invention, excellentrapid processability, color reproducibility, preserving ability in theunexposed state of a light-sensitive material, and image fastness wereexhibited.

Fifth Layer (Red-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion E 0.10 (gold-sulfur sensitized cubes, a 5:5 mixture of thelarge-size emulsion E-1 and the small-size emulsion E-2 (in terms of molof silver)) Gelatin 1.11 Cyan coupler (ExC-1) 0.02 Cyan coupler (ExC-3)0.01 Cyan coupler (ExC-4) 0.11 Cyan coupler (ExC-5) 0.01 Color-imagestabilizer (Cpd-1) 0.01 Color-image stabilizer (Cpd-6) 0.06 Color-imagestabilizer (Cpd-7) 0.02 Color-image stabilizer (Cpd-9) 0.04 Color-imagestabilizer (Cpd-10) 0.01 Color-image stabilizer (Cpd-14) 0.01Color-image stabilizer (Cpd-15) 0.12 Color-image stabilizer (Cpd-16)0.01 Color-image stabilizer (Cpd-17) 0.01 Color-image stabilizer(Cpd-18) 0.07 Color-image stabilizer (Cpd-20) 0.01 Ultraviolet absorbingagent (UV-7) 0.01 Solvent (Solv-5) 0.15 (ExC-4) Cyan coupler

(ExC-5) Cyan coupler

Example 3-6

The samples produced in Examples 3-1 to 3-5 were scan-exposed in thesame method as in Example 2-5, to evaluate the resulting samplesaccording to the method used in Examples 3-1 to 3-5. As a result, it wasfound that when the sample having the structure of the present inventionwas used, the effects of the present invention, such as excellent colorreproducibility and rapid processability, were exhibited particularlysignificantly.

Example 3-7

In the sample 109 described in Example 1 of JP-A-2001-142181, eachcomposition of the 15th layer, 16th layer and 17th layer was altered asshown below to prepare a sample.

15th Layer (Low Sensitivity Blue-Sensitive Emulsion Layer) Silverbromoiodide emulsion L silver 0.11 Silver bromoiodide emulsion M silver0.15 Gelatin 0.80 Yellow coupler (Exemplified compound (62) according to0.30 the present invention) Compound Cpd-M 0.01 High-boiling pointorganic solvent (Exemplified compound 0.05 (S-I-6) according to thepresent invention)

16th Layer (Middle Sensitivity Blue-Sensitive Emulsion Layer) Silverbromoiodide emulsion N silver 0.15 Silver bromoiodide emulsion O silver0.15 Gelatin 0.76 Yellow coupler (Exemplified compound (62) 0.34according to the present invention) Compound Cpd-N 0.002 High-boilingpoint organic solvent (Exemplified 0.06 compound (S-I-6) according tothe present invention)

17th Layer (High Sensitivity Blue-Sensitive Emulsion Layer) Silverbromoiodide emulsion O silver 0.15 Silver bromoiodide emulsion P silver0.15 Gelatin 1.10 Yellow coupler (Exemplified compound (62) 0.92according to the present invention) Compound Cpd-N 0.005 Compound Cpd-Q0.20 High-boiling point organic solvent (Exemplified 0.17 compound(S-I-6) according to the present invention)

In this connection, Silver bromoiodide emulsions L to P and CompoundsCpd-M, N and Q were the same as those described in Example 1 inJP-A-2001-142181.

Further, samples differing only in the point that the exemplifiedcompound (S-I-6) which was the high-boiling point organic solvent usedin each of the 15th layer, 16th layer and 17th layer was altered to anequal amount of compounds or mixtures were produced. As the compoundsand mixtures replaced for the exemplified compound (S-I-6), the solventsused in the first layer of the samples 3-111 to 3-130 of Example 3-1 ofthe present invention were used. Each of these samples was exposed tolight and processed (development processing A) by the method describedin Example 1 of Jp-A-2001-14²¹⁸¹. The humidity and heat fastness andlight fastness of each resulting sample were evaluated according to themethod described in Example 3-1 in the present specification, to confirmthe effects of the present invention.

Example 4-1 Preparation of Blue-Sensitive Emulsion A

To 1.06 liters of deionized distilled water containing 5.7 mass % ofdeionized gelatin were added 46.3 ml of a 10% solution of NaCl andfurther 46.4 ml of H₂SO₄ (1 N) and 0.012 g of a compound X. Then, theliquid temperature was adjusted to 60° C. when immediately 0.1 mol ofsilver nitrate and 0.1 mol of NaCl was added to the reaction vessel in10 minutes while performing high speed stirring. Subsequently, 1.5 molof silver nitrate and NaCl solution were added in 60 minutes by a flowrate increasing method so that a final addition rate became 4 times theinitial addition rate. Then, 0.2 mol % of silver nitrate and NaClsolution were added in 6 minutes at a constant addition rate. On thisoccasion, K₃IrCl₅(H₂O) was added to the NaCl solution in an amount of5×10⁻⁷ mol based on the total amount of silver to dope the grains withaquated iridium.

Further, 0.2 mol of silver nitrate and 0.18 mol of NaCl as well as 0.02mol of a KBr solution were added in 6 minutes. On this occasion,K₄Ru(CN)₆ and K₄Fe(CN)₆ corresponding to 0.5×10⁻⁵ mol based on the totalamount of silver were each added to the silver halide grains bydissolving them in the aqueous halogen solution.

Also, during growth of the grains in this final stage, an aqueous KIsolution corresponding to 0.001 mol based on the total amount of silverwas added into the reaction vessel in 1 minute. The addition was startedat a point in time when 93% of the total grains was formed.

Thereafter, the compound (Y) as a precipitant was added at 40° C. andthe pH was adjusted to about 3.5, and then the emulsion was desalted andwashed with water.

To the emulsion after the desalting and washing with water, deionizedgelatin and an aqueous NaCl solution as well as an aqueous NaOH solutionwere added and the temperature was elevated to 50° C. to adjust theemulsion to pAg 7.6 and pH 5.6.

Thus, a gelatin containing silver halide cubic grains having a halogencomposition of 98.9 mol % of silver chloride, 1 mol % of silver bromide,and 0.1 mol % of silver iodide, an average side length of 0.70 μm with avariation coefficient of side length being 8% was obtained.

The above-mentioned emulsion grains were maintained at 60° C. andSpectral sensitizing dye-1 and -2 were added thereto in amounts of2.5×10⁻⁴ mol/mol of Ag and 2.0×10⁻⁴ mol/mol of Ag, respectively.Further, Thiosulfonic acid compound 1 was added in an amount of 1×10⁻⁵mol/mol of Ag and then a fine grain emulsion containing 90 mol % ofsilver bromide and 10 mol % of silver chloride having an average graindiameter of 0.05 μm which was doped with iridium hexachloride was added,and the resultant was aged for 10 minutes. Further, fine grains of 40mol % of silver bromide and 60% of silver chloride having an averagegrain diameter of 0.05 μm was added thereto and aged for 10 minutes. Thefine grains were dissolved and as a result, the silver bromide contentof the host cubic grains increased to 1.3 mol. The iridium hexachloridewas doped in an mount of 1×10⁻⁷ mol/mol of Ag.

Subsequently, 1×10⁻⁵ mol/mol of Ag of sodium thiosulfate and 2×10⁻⁵mol/mol of Ag of Gold sensitizer-1 were added and immediately thereafterthe temperature was elevated to 60° C. and the mixture was subsequentlyaged for 40 minutes and then the temperature was decreased to 50° C.Immediately after the temperature decrease, Mercapto compound-1 and -2were added in amounts of 6×10⁻⁴ mol/mol of Ag, respectively. Then, after10 minutes of aging, an aqueous KBr solution was added to make 0.008 molbased on silver and after 10 minutes of aging, the temperature wasdecreased and the resultant was stored.

In this manner, a high sensitivity side emulsion A-1 was prepared.

In the same manner as described above except for the above-mentionedemulsion preparation method and temperature during the grain formation,cubic grains having an average side length of 0.55 μm with a variationcoefficient of side length being 9% were prepared. The temperatureduring the grain formation was 55° C.

The spectral sensitization and chemical sensitization were performed inamounts used for corrections performed to make specific surface areasequivalent (side length ratio of 0.7/0.55=1.27 times) to prepare a lowsensitivity side emulsion A-2.

(Preparation of Blue-Sensitive Emulsion B)

Among the conditions for preparing Emulsion A-1, the temperature duringthe grain formation was changed to 68° C. to make the grain size to anaverage side length of 0.85 μM. The variation coefficient of side lengthwas 12%. The introduction of iodide ions at the final stage of the grainformation was stopped and replaced by introduction of Cl ions.Therefore, the halogen composition at the time when the grain formationwas completed consisted of 99 mol % of silver chloride and 1 mol % ofsilver bromide.

The addition amounts of Spectral sensitizing dye-1 and Spectralsensitizing dye-2 were 1.25 times those at the time of preparingEmulsion A-1, respectively. Thiosulfonic acid compound-1 was used in theequivalent amount.

The chemical sensitization was changed as follows.

A fine grain emulsion containing silver halide grains having an averagegrain diameter of 0.05 μm and having a composition of 90 mol % of silverbromide and 10 mol % of silver chloride, doped with iridium hexachloridewas added and the resultant was aged for 10 minutes. Further, finegrains having an average grain diameter of 0.05 μm and having a silverhalide composition of 40 mol % of silver bromide and 60 mol % of silverchloride were added thereto and the resultant was aged for 10 minutes.The fine grains were dissolved and as a result the silver bromidecontent of ratio of the host cubic grains increased to 2.0 mol %. On theother hand, the iridium hexachloride was doped in an amount of 2×10⁻⁷mol/mol of Ag.

Subsequently, 1×10⁻⁵ mol/mol of Ag of sodium thiosulfate was added andimmediately thereafter the temperature was elevated to 55° C. and themixture was subsequently aged for 70 minutes and then the temperaturewas decreased to 50° C. No gold sensitizer was added.

Immediately after the temperature decrease, Mercapto compound-1 and -2were added in amounts of 4×10⁻⁴ mol/mol of Ag, respectively. Then, after10 minutes of aging, an aqueous KBr solution was added to make 0.010 molbased on silver and after 10 minutes of aging, the temperature wasdecreased and the resultant was stored.

In this manner a blue-sensitive high sensitivity side emulsion B-1 forcomparison was prepared.

In the same manner as the Emulsion B-1, grains having an average sidelength of 0.68 μm with a variation coefficient of side length being 12%was prepared by decreasing the temperature at the time of grainformation.

The spectral sensitizer and chemical sensitizer were used in amounts of1.25 times those of Emulsion B-1 taking into consideration of the ratioof surface areas, to prepare a low sensitivity side emulsion B-2.

(Preparation of Inventive Green Sensitive Layer Emulsions C-1 and C-2)

Under the same preparation conditions for emulsions A-1 and A-2, exceptthat the temperature at the time of forming grains was lowered, and thekind of sensitizing dyes were changed as described below, a greensensitive layer (GL) high-sensitivity emulsion C-1 and a green sensitivelayer (GL) low-sensitivity emulsion C-2 were prepared.

As for the grain size, the high-sensitivity emulsion C-1 had the averageside length of 0.40 μm and the low-sensitivity emulsion C-2 had theaverage side length of 0.30 μm, each with the variation coefficient ofaverage length of 8%.

The sensitizing dye D was added to the large-size emulsion(high-sensitivity emulsion C-1) in an amount of 3.0×10⁻⁴ mol, and to thesmall-size emulsion (low-sensitivity emulsion C-2) in an amount of3.6×10⁻⁴ mol, per mol of the silver halide; and the sensitizing dye Ewas added to the large-size emulsion in an amount of 4.0×10⁻⁵ mol, andto the small-size emulsion in an amount of 7.0×10⁻⁵ mol, per mol of thesilver halide.

(Preparation of Inventive Green Sensitive Layer Emulsions D-1 and D-2)

Under the same preparation conditions for emulsions B-1 and B-2, exceptthat the temperature at the time of forming grains was lowered, and thekind of sensitizing dyes were changed as described below, a greensensitive layer high-sensitivity emulsion D-1 and a green sensitivelayer low-sensitivity emulsion D-2 were prepared.

As for the grain size, the high-sensitivity emulsion C-1 had the averageside length of 0.50 μm and the low-sensitivity emulsion C-2 had theaverage side length of 0.40 μm, each with the variation coefficient ofaverage length of 10%, respectively.

The sensitizing dye D was added to the large-size emulsion(high-sensitivity emulsion C-1) in an amount of 4.0×10⁻⁴ mol, and to thesmall-size emulsion (low-sensitivity emulsion C-2) in an amount of4.5×10⁻⁴ mol, per mol of the silver halide; and the sensitizing dye Ewas added to the large-size emulsion in an amount of 5.0×10⁻⁵ mol, andto the small-size emulsion in an amount of 8.8×10⁻⁵ mol, per mol of thesilver halide.

(Preparation of Inventive Red Sensitive Layer Emulsions E-1 and E-2)

Under the same preparation conditions for emulsions A-1 and A-2, exceptthat the temperature at the time of forming grains was lowered, and thekind of sensitizing dyes were changed as described below, a redsensitive layer high-sensitivity emulsion E-1 and a red sensitive layerlow-sensitivity emulsion E-2 were prepared.

As for the grain size, the high-sensitivity emulsion E-1 had the averageside length of 0.38 μm and the low-sensitivity emulsion E-2 had theaverage side length of 0.32 μm, with the variation coefficient ofaverage length of 9% and 10%, respectively.

The sensitizing dyes G and H were added to the large-size emulsion(high-sensitivity emulsion E-1) in an amount of 8.0×10⁻⁵ mol, and to thesmall-size emulsion (low-sensitivity emulsion E-2) in an amount of10.7×10⁻⁵ mol, per mol of the silver halide, respectively.

Further, Compound I below was added to red sensitive layer in an amountof 3.0×10⁻³ mol.

(Preparation of Inventive Red Sensitive Layer Emulsions F-1 and F-2)

Under the same preparation conditions for emulsions B-1 and B-2, exceptthat the temperature at the time of forming grains was lowered, and thekind of sensitizing dyes were changed as described below, a redsensitive layer high-sensitivity emulsion F-1 and a red sensitive layerlow-sensitivity emulsion F-2 were prepared.

As for the grain size, the high-sensitivity emulsion F-1 had the averageside length of 0.57 μm and the low-sensitivity emulsion F-2 had theaverage side length of 0.43 μm, with the variation coefficient ofaverage length of 9% and 10%, respectively.

The sensitizing dyes G and H were added to the large-size emulsion(high-sensitivity emulsion F-1) in an amount of 1.0×10⁻⁴ mol, and to thesmall-size emulsion (low-sensitivity emulsion F-2) in an amount of1.34×10⁻⁴ mol, per mol of the silver halide, respectively.

Further, Compound I was added to red sensitive emulsion layer in anamount of 3.0×10⁻³ mol.

(Preparation of a Coating Solution for the First Layer)

Into 21 g of a solvent (Solv-1) and 80 ml of ethyl acetate weredissolved 57 g of a yellow coupler (ExY), 7 g of a color-imagestabilizer (Cpd-1), 4 g of a color-image stabilizer (Cpd-2), 7 g of acolor-image stabilizer (Cpd-3), and 2 g of a color-image stabilizer(Cpd-8). This solution was emulsified and dispersed in 220 g of a 23.5mass % aqueous gelatin solution containing 4 g of sodiumdodecylbenzenesulfonate with a high-speed stirring emulsifier(dissolver). Water was added thereto, to prepare 900 g of an emulsifieddispersion A.

On the other hand, the above emulsified dispersion A and the prescribedemulsions A-1 and A-2 were mixed and dissolved, and the first-layercoating solution was prepared so that it would have the compositionshown below. The coating amount of the emulsion is in terms of silver.

The coating solutions for the second layer to the seventh layer wereprepared in the similar manner as that for the first-layer coatingsolution. As a gelatin hardener for each layer,1-oxy-3,5-dichloro-s-triazine sodium salt (H-1), (H-2), and (H-3) wereused. Further, to each layer, were added Ab-1, Ab-2, Ab-3, and Ab-4, sothat the total amounts would be 15.0 mg/m², 60.0 mg/m², 5.0 mg/m², and10.0 mg/m², respectively. (H-1) Hardener

(H-2) Hardener

(H-3) Hardener

(Ab-1) Antiseptic

(Ab-2) Antiseptic

(Ab-3) Antiseptic

(Ab-4) Antiseptic

R₁ R₂ a —CH₃ —NHCH₃ b —CH₃ —NH₂ c —H —NH₂ d —H —NHCH₃A mixture in 1:1:1:1 (molar ratio) of a, b, c, and d

Further, to the second layer, the fourth layer, the sixth layer, and theseventh layer, was added 1-(3-methylureidophenyl)-5-mercaptotetrazole inamounts of 0.2 mg/m², 0.2 mg/m², 0.6 mg/m², and 0.1 mg/m², respectively.

Further, to the blue-sensitive emulsion layer and the green-sensitiveemulsion layer, was added 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene inamounts of 1×10⁻⁴ mol and 2×10⁻⁴ mol, respectively, per mol of thesilver halide.

Further, to the red-sensitive emulsion layer, was added a copolymerlatex of methacrylic acid and butyl:acrylate (1:1 in mass ratio; averagemolecular weight, 200,000 to 400,000) in an amount of 0.05 g/m².Disodium salt of catecol-3,5-disulfonic acid was added to the secondlayer, the fourth layer and the sixth layer so that coating amountswould be 6 mg/m², 6 mg/m² and 18 mg/m², respectively.

Further, in order to prevent irradiation, the following dyes (coatingamounts are shown in parentheses) were added.

(Layer Constitution)

The composition of each layer is shown below. The numbers show coatingamounts (g/m²). In the case of the silver halide emulsion, the coatingamount is in terms of silver.

Support

Polyethylene Resin-Laminated Paper

-   -   (The polyethylene resin on the first layer side contained a        white pigment (TiO₂; content of 16 mass %, znO; content of 4        mass %), a fluorescent whitening agent        (4,4′-bis(5-methylbenzoxazolyl)stilbene; content of 0.03 mass %)        and a bluish dye (ultramarine; content of 0.33 mass %). The        amount of the polyethylene resin was 29.2 g/m²

First Layer (Blue-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion A (gold-sulfur 0.24 sensitized cubes, a 3:7 mixture of thelarge-size emulsion A-1 and the small-size emulsion A-2 (in terms of molof silver)) Gelatin 1.25 Yellow coupler (ExY-1) 0.57 Color-imagestabilizer (Cpd-1) 0.07 Color-image stabilizer (Cpd-2) 0.04 Color-imagestabilizer (Cpd-3) 0.07 Color-image stabilizer (Cpd-8) 0.02 Solvent(Solv-1) 0.21

(Average Size of Grain in Emulsion: 0.15 μm)

Second Layer (Color-Mixing Inhibiting Layer) Gelatin 1.15 Color-mixinginhibitor (Cpd-4) 0.10 Color-image stabilizer (Cpd-5) 0.018 Color-imagestabilizer (Cpd-6) 0.13 Color-image stabilizer (Cpd-7) 0.07 Solvent(Solv-1) 0.04 Solvent (Solv-2) 0.12 Solvent (Solv-5) 0.11

Third Layer (Green-sensitive Emulsion Layer) Silver chloroiodobromideemulsion C 0.14 (gold-sulfur sensitized cubes, a 1:3 mixture of thelarge-size emulsion C-1 and the small-size emulsion C-2 (in terms of molof silver)) Gelatin 0.46 Magenta coupler (ExM) 0.15 Ultravioletabsorbing agent (UV-A) 0.14 Color-image stabilizer (Cpd-2) 0.003Color-mixing inhibitor (Cpd-4) 0.002 Color-image stabilizer (Cpd-6) 0.09Color-image stabilizer (Cpd-8) 0.02 Color-image stabilizer (Cpd-9) 0.01Color-image stabilizer (Cpd-10) 0.01 Color-image stabilizer (Cpd-11)0.0001 Solvent (Solv-3) 0.09 Solvent (Solv-4) 0.18 Solvent (Solv-5) 0.17

(Average Size of Grain in Emulsion: 0.25 μm)

Fourth Layer (Color-Mixing Inhibiting Layer) Gelatin 0.68 Color-mixinginhibitor (Cpd-4) 0.06 Color-image stabilizer (Cpd-5) 0.011 Color-imagestabilizer (Cpd-6) 0.08 Color-image stabilizer (Cpd-7) 0.04 Solvent(Solv-1) 0.02 Solvent (Solv-2) 0.07 Solvent (Solv-5) 0.065

Fifth Layer (Red-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion E 0.16 (gold-sulfur sensitized cubes, a 5:5 mixture of thelarge-size emulsion E-1 and the small-size emulsion E-2 (in terms of molof silver)) Gelatin 0.95 Cyan coupler (ExC-1) 0.023 Cyan coupler (ExC-2)0.05 Cyan coupler (ExC-3) 0.17 Ultraviolet absorbing agent (UV-A) 0.055Color-image stabilizer (Cpd-1) 0.22 Color-image stabilizer (Cpd-7) 0.003Color-image stabilizer (Cpd-9) 0.01 Color-image stabilizer (Cpd-12) 0.01Solvent (Solv-8) 0.05

(Average Size of Grain in Emulsion: 0.19 μm)

Sixth Layer (Ultraviolet Absorbing Layer) Sixth Layer (UltravioletAbsorbing Layer) Gelatin 0.46 Ultraviolet absorbing agent (UV-B) 0.35Compound (S1-4) 0.0015 Solvent (Solv-7) 0.18 Seventh Layer (ProtectiveLayer) Gelatin 1.00 Acryl-modified copolymer of polyvinyl alcohol 0.4(modification degree: 17%) Liquid paraffin 0.02 Surface-active agent(Cpd-13) 0.02 (ExY-1) Yellow coupler

(ExY-2)

(ExY-3)

(ExM) Magenta coupler A mixture in 50:50 (molar ratio) of

(ExC-1) Cyan coupler

(ExC-2) Cyan coupler

(ExC-3) Cyan coupler

(ExC-4) Cyan coupler

(ExC-5) Cyan coupler

(Cpd-1) Color-image stabilizer

number-average molecular weight 60,000 (Cpd-2) Color-image stabilizer

(Cpd-3) Color-image stabilizer

n = 7˜8 (average value) (Cpd-4) Color-mixing inhibitor

(Cpd-5) Color-image stabilizer

(Cpd-6) Color-image stabilizer

number-average molecular weight 600 m/n = 10/90 (Cpd-7) Color-imagestabilizer

(Cpd-8) Color-image stabilizer

(Cpd-9) Color-image stabilizer

(Cpd-10) Color-image stabilizer

(Cpd-11)

(Cpd-12)

(Cpd-13) Surface-active agent A mixture in 6:2:2 (molar ratio) of

(Cpd-15)

(Cpd-18)

(Cpd-19)

(Cpd-20)

(UV-1) Ultraviolet absorbing agent

(UV-2) Ultraviolet absorbing agent

(UV-3) Ultraviolet absorbing agent

(UV-5) Ultraviolet absorbing agent

(UV-6) Ultraviolet absorbing agent

(UV-7) Ultraviolet absorbing agent

UV-A A mixture of UV-1/UV-2/UV-3 = 7/2/2 (mass ratio) UV-B A mixture ofUV-1/UV-2/UV-3/UV-5/UV-6 = 13/3/3/5/3 (mass ratio) UV-C A mixture ofUV-1/UV-3 = 9/1 (mass ratio) (Solv-1)

(Solv-2)

(Solv-3)

(Solv-4)

(Solv-5)

(Solv-7)

(Solv-8)

(Solv-9)

(Solv-10)

(S1-4)

(Solv-11)

(m, p) (Solv-12)

(Solv-13) Oleyl alcohol

In the sample 4-001 produced in the above manner, changing was conductedas shown below to produce a sample.

Preparation of Sample 4-101

A sample 4-101 was prepared in the same manner as for sample 4-001,except that the compositions of the first, third and fifth layers of theabove-mentioned sample 4-001 were changed as described below.

First Layer (Blue-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion (a 3:7 mixture of the 0.21 emulsion B-H and the emulsion B-L(in terms of mol of silver)) Gelatin 1.00 Yellow coupler (ExY-1) 0.57Color-image stabilizer (Cpd-1) 0.07 Color-image stabilizer (Cpd-2) 0.04Color-image stabilizer (Cpd-3) 0.07 Color-image stabilizer (Cpd-8) 0.02Solvent (Solv-1) 0.35

(Average Size of Grain in Emulsion: 0.08 μm)

Further, the silver chloroiodobromide emulsions (Emulsion B-H andEmulsion B-L) were prepared in the same manner as in Example 2-4described above.

Third Layer (Green-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion 0.12 (a 1:3 mixture of the emulsion G-H and the emulsion G-L(in terms of mol of silver)) Gelatin 0.36 Magenta coupler (ExM) 0.12Color-image stabilizer (Cpd-2) 0.003 Color-mixing inhibitor (Cpd-4)0.002 Color-image stabilizer (Cpd-6) 0.16 Color-image stabilizer (Cpd-8)0.02 Color-image stabilizer (Cpd-9) 0.01 Color-image stabilizer (Cpd-10)0.01 Color-image stabilizer (Cpd-11) 0.0001 Solvent (Solv-11) 0.08Solvent (Solv-12) 0.16 Solvent (Solv-13) 0.11

(Average Size of Grain in Emulsion: 0.08 μm)

Further, the silver chloroiodobromide emulsions (Emulsion G-H andEmulsion G-L) were prepared in the same manner as in Example 2-4described above.

Fifth Layer (Red-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion 0.10 (a 5:5 mixture of the emulsion R-H and the emulsion R-L(in terms of mol of silver)) Gelatin 0.95 Cyan coupler (ExC-1) 0.10 Cyancoupler (ExC-3) 0.05 Cyan coupler (ExC-5) 0.01 Color-image stabilizer(Cpd-6) 0.01 Color-image stabilizer (Cpd-7) 0.02 Color-image stabilizer(Cpd-9) 0.04 Color-image stabilizer (Cpd-10) 0.01 Color-image stabilizer(Cpd-15) 0.16 Color-image stabilizer (Cpd-18) 0.04 Color-imagestabilizer (Cpd-20) 0.01 Ultraviolet absorbing agent (UV-7) 0.07 Solvent(Solv-5) 0.19

(Average Size of Grain in Emulsion: 0.15 μm)

Further, the silver chloroiodobromide emulsions (Emulsion R-H andEmulsion R-L) were prepared in the same manner as in Example 2-4described above.

Preparation of Sample 4-201

A sample 4-201 was prepared in the same manner, except that thecomposition of the first layer of the sample 4-101 was changed asdescribed below.

First Layer (Blue-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion (a 3:7 mixture of the 0.13 emulsion B-H and the emulsion B-L(in terms of mol of silver)) Gelatin 1.00 Yellow coupler (ExY-2) 0.34Color-image stabilizer (Cpd-2) 0.07 Color-image stabilizer (Cpd-8) 0.08Color-image stabilizer (Cpd-20) 0.08 Solvent (Solv-11) 0.35

(Average size of grain in emulsion: 0.08 μm)

Preparation of Sample 4-301

A sample 4-301 was prepared in the same manner, except that thecomposition of the third layer of the sample 4-101 was changed asdescribed below.

Third Layer (Green-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion 0.10 (a 1:3 mixture of the emulsion G-H and the emulsion G-L(in terms of mol of silver)) Gelatin 0.36 Magenta coupler (ExM) 0.14Color-image stabilizer (Cpd-2) 0.004 Color-mixing inhibitor (Cpd-4)0.002 Color-image stabilizer (Cpd-6) 0.19 Color-image stabilizer (Cpd-8)0.02 Color-image stabilizer (Cpd-9) 0.01 Color-image stabilizer (Cpd-10)0.01 Color-image stabilizer (Cpd-11) 0.0001 Solvent (Solv-11) 0.10Solvent (Solv-12) 0.19 Solvent (Solv-13) 0.13

(Average size of grain in emulsion: 0.08 μm)

Preparation of Sample 4-401

A sample 4-401 was prepared in the same manner, except that thecomposition of the third layer of the sample 4-101 was changed asdescribed below.

Third Layer (Green-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion 0.08 (a 1:3 mixture of the emulsion G-H and the emulsion G-L(in terms of mol of silver)) Gelatin 0.36 Magenta coupler (ExM) 0.18Color-image stabilizer (Cpd-2) 0.004 Color-mixing inhibitor (Cpd-4)0.002 Color-image stabilizer (Cpd-6) 0.19 Color-image stabilizer (Cpd-8)0.02 Color-image stabilizer (Cpd-9) 0.01 Color-image stabilizer (Cpd-10)0.01 Color-image stabilizer (Cpd-11) 0.0001 Solvent (Solv-11) 0.20Solvent (Solv-12) 0.32 Solvent (Solv-13) 0.50

(Average size of grain in emulsion: 0.06 μm)

Preparation of Sample 4-501

A sample 4-501 was prepared in the same manner, except that thecompositions of the first layer and the fifth layer of the sample 4-101were changed as described below.

First Layer (Blue-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion (a 3:7 mixture of the 0.21 emulsion B-H and the emulsion B-L(in terms of mol of silver)) Gelatin 1.00 Yellow coupler (ExY-3) 0.42Color-image stabilizer (Cpd-1) 0.07 Color-image stabilizer (Cpd-2) 0.04Color-image stabilizer (Cpd-3) 0.07 Color-image stabilizer (Cpd-8) 0.02Solvent (Solv-1) 0.35

(Average Size of Grain in Emulsion: 0.08 μm)

Fifth Layer (Red-Sensitive Emulsion Layer) Silver chloroiodobromideemulsion 0.09 (a 5:5 mixture of the emulsion R-H and the emulsion R-L(in terms of mol of silver)) Gelatin 1.11 Cyan coupler (ExC-1) 0.14Color-image stabilizer (Cpd-6) 0.01 Color-image stabilizer (Cpd-9) 0.04Color-image stabilizer (Cpd-10) 0.01 Color-image stabilizer (Cpd-15)0.20 Color-image stabilizer (Cpd-18) 0.07 Ultraviolet absorbing agent(UV-7) 0.07 Solvent (Solv-5) 0.50

(Average Size of Grain in Emulsion: 0.07 μm)

Each sample was stored at 25° C. and 55% RH for 10 days after thecoating, and then the sample was exposed to light from a conventional Xelight source through a filter that spectrally separates the light intored, green and blue and a 20-stage wedge on HIE type sensitometermanufactured by Fuji Photo Film Co., Ltd. with applying a voltage of1,000 v to a capacitor in an amount of exposure to light correspondingto 0.0001 second 200,000 1× sec. After the exposed sample was stored for30 minutes under the conditions of 25° C. and 55% RH, each sample wasprocessed with color-development processing A described hereinbelow.

Color-Development Processing Step A

Each photosensitive material sample described above was processed into aform of a roll with a width of 127 mm, and the photosensitive materialwas imagewise exposed from a negative film of average density, by usinga laboratory processor obtained by modifying Mini Labo Printer ProcessorPP350 manufactured by Fuji Photo Film Co., Ltd. so that the processingtime and processing temperature could be changed, and continuousprocessing (running test) was performed until the volume of thecolor-developer replenisher used in the following processing step becamedouble the volume of the color-developer tank. The processing using thisrunning processing solution was named processing A. Processing stepTemperature Time Replenishment rate* Color development 45.0° C. 15 sec 45 ml Bleach-fixing 40.0° C. 15 sec 35 ml Rinse (1) 40.0° C. 6 sec —Rinse (2) 40.0° C. 6 sec — Rinse (3)** 40.0° C. 6 sec — Rinse (4)**38.0° C. 6 sec 121 ml  Drying   80° C. 15 sec (Notes)*Replenishment rate per m² of the light-sensitive material to beprocessed.**A rinse cleaning system RC50D, trade name, manufactured by Fuji PhotoFilm Co., Ltd., was installed in the rinse (3), and the rinse solutionwas taken out from the rinse (3) and sent to a reverse osmosis membranemodule (RC50D) by using a pump. The permeated water obtained in thattank was supplied to the rinse (4), and the concentrated water wasreturned to the rinse (3). Pump pressure was controlled such that thewater to be permeated in the reverse osmosis module would be maintained# in an amount of 50 to 300 ml/min, and the rinse solution wascirculated under controlled temperature for 10 hours a day. The rinsewas made in a tank counter-current system from (1) to (4).

The composition of each processing solution was as follows. (Colordeveloper) (Tank solution) (Replenisher) Water 800 ml 800 ml Fluorescentwhitening agent (FL-3) 4.0 g 8.0 g Residual color reducing agent 3.0 g5.5 g (SR-1) Triisopropanolamine 8.8 g 8.8 g Sodium p-toluenesulfonate10.0 g 10.0 g Ethylenediamine tetraacetic acid 4.0 g 4.0 g Sodiumsulfite 0.10 g 0.10 g Potassium chloride 10.0 g — Sodium4,5-dihydroxybenzene- 0.50 g 0.50 g 1,3-disulfonateDisodium-N,N-bis(sulfonatoethyl) 8.5 g 14.0 g hydroxylamine4-amino-3-methyl-N-ethyl-N- 7.0 g 19.0 g(β-methanesulfonamidoethyl)aniline •3/2 sulfate•monohydrate Potassiumcarbonate 26.3 g 26.3 g Water to make 1000 ml 1000 ml pH (25° C.,adjusted using sulfuric 10.25 12.6 acid and potassium hydroxide)

(Bleach-fixing solution) (Tank solution) (Replenisher) Water 800 ml 800ml Ammonium thiosulfate (750 g/l) 107 ml 214 ml Succinic acid 29.5 g59.0 g Ammonium iron (III) 47.0 g 94.0 g ethylenediaminetetraacetateEthylenediaminetetraacetic acid 1.4 g 2.8 g Nitric acid (67%) 17.5 g35.0 g Imidazole 14.6 g 29.2 g Ammonium sulfite 16.0 g 32.0 g Potassiummetabisulfite 23.1 g 46.2 g Water to make 1000 ml 1000 ml pH (25° C.,adjusted using nitric 6.00 6.00 acid and aqueous ammonia)

(Rinse solution) (Tank solution) (Replenisher) Sodiumchlorinated-isocyanurate 0.02 g 0.02 g Deionized water 1000 ml 1000 ml(conductivity: 5 μS/cm or less) pH (25° C.) 6.5 6.5

Each sample thus processed were measured for the density of a yellowcomponent, D_(y), the density of a magenta component, D_(m), and thedensity of a cyan component, D_(c), by determining the density of eachpatch stepwise exposed by use of an X-rite, and a sensitometry curve wasprepared from the measured densities by complementing gaps between therespective measuring points. Similarly, gray stepwise exposure wasperformed such that neutrality was reached at a density of 0.7 byadjusting with a gelatin color filter without resort to color separationand passing the sample through the above-mentioned color-developmentprocessing A. Then, the color-development processing B was performed andthe density was measured by use of X-rite. The density of the yellowcomponent was named D_(gy), the density of the magenta component wasnamed D_(gm), and the density of the cyan component was named D_(gc).

As an index of rapid high-productivity processing suitability, the linespeed of color development processing was set from 10 seconds to 30seconds at an interval of 1 second and the time t_(2.0) in which all ofthe densities, D_(gy), D_(gm), and D_(gc), reached 2.0 was examined. Thesmaller the time t_(2.0) is, the more rapid high-productivity processingsuitability the sample has. Here, t_(2.0) was obtained by interpolationor extrapolation from the experimental data.

Also, as an index for color separation, the values of Dc and D_(y) atdensity points that give D_(m)=2.0 of a green-separated exposed patchare defined as D_(c/m) and D_(y/m), respectively, and the value of D_(m)at the density point that gives D_(y)=2.0 of a blue-separated exposedpatch was defined as Dm/y, and evaluation of color mixing was performed.

To evaluate the color stain with a lapse of time, a nonexposed samplewas passed through color-development processing A and then themeasurement of density of a white background portion was performed byuse of X-rite and the initial white background densities were defined asD_(sy), D_(sm), and D_(sc), respectively. Further, after each sample wasstored at 35° C. and 60% RH for 3 months in the dark, again the densitythereof was measured by use of X-rite and density increments ofrespective color components were defined as D_(Δsy), D_(Δsm) andD_(Δsc), respectively. The lower the initial white background densityis, and the smaller the increase in the density is, the more preferredthe sample is.

Samples 4-102, 4-103, 4-202, 4-203, 4-302, 4-303, 4-402, 4-403, 4-502and 4-503 as shown in Table 16 were prepared in the same manner asdescribed above, except that the coating flow rates of the color mixingpreventing layers in Samples 4-001 to 4-501 were changed (changes inflow rate meaning changes in coating amounts), respectively. Then, thesesamples were measured of rapid processability, t_(2.0), color mixingdensities, D_(c/m), D_(y/m) and D_(m/y), white background densities,D_(sy), D_(sm) and D_(sc), coloring densities with a lapse of time,D_(Δsy), D_(Δsm) and D_(Δsc) stain, and average relative coupling rates,kar, of each of the yellow color-forming layer, magenta color-forminglayer, and cyan color-forming layer (obtained by the method describedherein at 20 measuring points with the densities of dye being determinedby extraction and the bleach fixing and subsequent operations beingperformed according to processing B in Example 4-3 describedhereinbelow).

Table 17 shows the results obtained. TABLE 16 Coating flow rate Coatingflow rate No. of sample Sample of the second of the fourth which wasSilver coating Gelatin coating No. layer (%) layer (%) modified amount(g/m²) amount (g/m²) 4-001 100 100 4-001 0.54 5.95 4-002 70 90 4-0010.54 5.54 4-101 100 100 4-101 0.43 5.60 4-102 70 90 4-101 0.43 5.194-103 45 75 4-101 0.43 4.80 4-201 100 100 4-201 0.35 5.60 4-202 70 904-201 0.35 5.19 4-203 45 75 4-201 0.35 4.80 4-301 100 100 4-301 0.415.60 4-302 70 90 4-301 0.41 5.19 4-303 45 75 4-301 0.41 4.80 4-401 100100 4-401 0.39 5.60 4-402 70 90 4-401 0.39 5.19 4-403 45 75 4-401 0.394.80 4-501 100 100 4-501 0.42 5.60 4-502 70 90 4-501 0.42 5.19 4-503 200200 4-501 0.42 7.43

TABLE 17 Kar Sample No. Y M C t_(2.0) Dc/m Dy/m Dm/y D_(sy) D_(sm)D_(sc) D_(Δsy) D_(Δsm) D_(Δsc) 4-001 1.00 0.55 1.25 12.5 0.20 0.32 0.280.10 0.11 0.08 0.03 0.02 0.01 4-002 1.01 0.57 1.26 12.1 0.21 0.33 0.300.10 0.11 0.08 0.03 0.02 0.01 4-101 1.05 0.67 1.34 8.0 0.18 0.31 0.240.09 0.10 0.07 0.02 0.01 0.01 4-102 1.07 0.69 1.34 7.8 0.18 0.31 0.250.09 0.10 0.07 0.02 0.01 0.01 4-103 1.09 0.70 1.35 7.6 0.20 0.32 0.270.08 0.09 0.08 0.01 0.01 0.01 4-201 1.18 0.66 1.34 6.8 0.18 0.30 0.260.10 0.10 0.07 0.02 0.01 0.01 4-202 1.19 0.67 1.35 6.6 0.19 0.31 0.270.10 0.10 0.07 0.02 0.01 0.01 4-203 1.19 0.67 1.35 6.3 0.20 0.32 0.280.09 0.10 0.08 0.01 0.02 0.01 4-301 1.04 0.75 1.34 7.5 0.18 0.30 0.240.09 0.10 0.07 0.02 0.01 0.01 4-302 1.05 0.77 1.34 7.3 0.18 0.31 0.250.09 0.10 0.07 0.01 0.01 0.01 4-303 1.06 0.79 1.34 7.1 0.19 0.31 0.270.08 0.09 0.08 0.01 0.01 0.01 4-401 1.04 0.80 1.35 7.1 0.18 0.29 0.240.09 0.10 0.07 0.02 0.01 0.01 4-402 1.05 0.82 1.35 6.9 0.18 0.29 0.250.08 0.09 0.07 0.01 0.01 0.01 4-403 1.05 0.83 1.35 6.7 0.18 0.31 0.270.08 0.09 0.07 0.01 0.01 0.01 4-501 2.24 0.65 2.08 6.5 0.32 0.41 0.260.14 0.12 0.11 0.12 0.03 0.08 4-502 2.23 0.67 2.09 6.2 0.35 0.49 0.260.14 0.12 0.11 0.11 0.02 0.07 4-503 2.25 0.67 2.08 12.6 0.22 0.35 0.270.16 0.13 0.12 0.09 0.02 0.08

Note that R in the table above indicates a cyan color-forming layer, Gindicates a magenta color-forming layer, and B indicates a yellowcolor-forming layer.

As compared with Samples 4-001 and 4-002 in Table 17, Samples 4-101 to4-403 had shortened t_(2.0), while they had decreased D_(c/m), D_(y/m)and D_(m/y), that is, they had an improved color separability whilehaving rapid processing suitability. Further, no deterioration wasobserved in the white background density D_(sy), D_(sm) and D_(sc), orin the color densities with a lapse of time, D_(Δsy), D_(Δsm) andD_(Δsc) stain. On the other hand, it was revealed that Samples 4-501 and4-502 showed shortening of t_(2.0), but the color separability wasdeteriorated. Further, it was revealed that Sample 4-503 of which thecolor mixing preventing ability was increased in order to improve thecolor separability underwent deterioration of t_(2.0), so that it didnot have rapid processing suitability and setting the average relativecoupling rate, kar, at a high level was found to be not preferable. Itwas demonstrated that setting the average relative coupling rate, kar,in the range stipulated by the present invention enabled imparting rapidprocessing suitability while improving the color separation.

Example 4-2

The order of the layers constituting the silver halideemulsion-containing layers of Samples 4-101 and 4-201 described inExample 4-1 was changed as shown in Table 18 and rapid processabilityt_(2.0) and color mixing densities, D_(c/m), D_(y/m) and D_(m/y), weremeasured. The results obtained are shown in Table 19. TABLE 18 Coatingflow Coating flow rate of rate of No. of sample Fifth layer/third Samplethe second the fourth which was layer/first No. layer (%) layer (%)modified layer 4-001 100 100 4-001 R/G/B 4-101 100 100 4-101 R/G/B 4-10270 90 4-101 R/G/B 4-103 45 75 4-101 R/G/B 4-104 100 100 4-101 G/R/B4-105 70 90 4-101 G/R/B 4-106 45 75 4-101 G/R/B 4-201 100 100 4-201R/G/B 4-202 70 90 4-201 R/G/B 4-203 45 75 4-201 R/G/B 4-204 100 1004-201 G/R/B 4-205 70 90 4-201 G/R/B 4-206 45 75 4-201 G/R/B 4-207 100100 4-201 B/R/G 4-208 70 90 4-201 B/R/G

TABLE 19 Kar Fifth layer/ Sample No. Y M C third layer/first layert_(2.0) D_(c/m) D_(y/m) D_(m/y) 4-001 0.99 0.55 1.25 R/G/B 12.5 0.200.32 0.28 4-101 1.05 0.67 1.34 R/G/B 8.0 0.18 0.31 0.24 4-102 1.05 0.671.34 R/G/B 7.8 0.18 0.31 0.25 4-103 1.05 0.67 1.34 R/G/B 7.6 0.20 0.320.27 4-104 1.05 0.67 1.34 G/R/B 6.2 0.18 0.29 0.24 4-105 1.05 0.67 1.34G/R/B 6.0 0.18 0.29 0.24 4-106 1.05 0.67 1.34 G/R/B 5.8 0.19 0.29 0.244-201 1.18 0.66 1.34 R/G/B 6.8 0.18 0.30 0.26 4-202 1.18 0.66 1.34 R/G/B6.6 0.19 0.31 0.27 4-203 1.18 0.66 1.34 R/G/B 6.3 0.20 0.32 0.28 4-2041.18 0.66 1.34 G/R/B 5.5 0.18 0.29 0.24 4-205 1.18 0.66 1.34 G/R/B 5.20.19 0.29 0.24 4-206 1.18 0.66 1.34 G/R/B 4.9 0.20 0.29 0.24 4-207 1.180.66 1.34 B/R/G 5.8 0.19 0.29 0.24 4-208 1.18 0.66 1.34 B/R/G 5.6 0.200.29 0.25

Comparison of Samples 4-101 to 4-103 with Samples 4-104 to 4-106 inTable 19 revealed that t_(2.0) was greatly shortened while D_(c/m),D_(y/m) and D_(m/y) were decreased. This indicates that locating thered-sensitive emulsion layer having a high average relative couplingrate, kar, as the third layer imparts the photographic light-sensitivematerial with rapid processing suitability while it further improved thecolor separability. Further, comparison between Samples 4-201 to 4-203with Samples 4-204 to 4-208 showed similar results. From the above, itwas revealed that locating the emulsion layer of which the averagerelative coupling rate, kar, was the highest among the three silverhalide-containing emulsion layers between the color mixinginhibitor-containing layers so as to be sandwiched thereby enabledimparting rapid processing suitability while improving the colorseparability.

Example 4-3

Similar evaluations performed in the same manner as in Examples 4-1 and4-2, except that the color-development processing A was changed to thefollowing color-development processing B gave similar results.

Color-Developing Processing Step B

Each of the samples above was processed into a form of a roll with awidth of 127 mm, and the photosensitive material sample was imagewiseexposed from a negative film of average density, by using Mini LaboPrinter Processor PP350 manufactured by Fuji Photo Film Co., Ltd., andcontinuous processing (running test) was performed until the volume ofthe color-developer replenisher used in the following processing stepbecame double the volume of the color-developer tank. The processingusing this running processing solution was named processing B.Replenishment Processing step Temperature Time rate* Color development38.5° C. 45 sec 45 ml Bleach-fixing 38.0° C. 45 sec 35 ml Rinse (1)38.0° C. 20 sec — Rinse (2) 38.0° C. 20 sec — Rinse (3)** 38.0° C. 20sec — Rinse (4)** 38.0° C. 20 sec 121 ml  Drying   80° C.(Notes)*Replenishment rate per m² of the light-sensitive material to beprocessed.**A rinse cleaning system RC50D, trade name, manufactured by Fuji PhotoFilm Co., Ltd., was installed in the rinse (3), and the rinse solutionwas taken out from the rinse (3) and sent to a reverse osmosis membranemodule (RC50D) by using a pump. The permeated water obtained in thattank was supplied to the rinse (4), and the concentrated water wasreturned to the rinse (3). Pump pressure was controlled such that thewater to be permeated in the reverse osmosis module would be#maintained in an amount of 50 to 300 ml/min, and the rinse solution wascirculated under controlled temperature for 10 hours a day. The rinsewas made in a tank counter-current system from (1) to (4).

The composition of each processing solution was as follows. (Colordeveloper) (Tank solution) (Replenisher) Water 800 ml 800 ml Fluorescentwhitening agent (FL-1) 2.2 g 5.1 g Fluorescent whitening agent (FL-2)0.35 g 1.75 g Triisopropanolamine 8.8 g 8.8 g Polyethylene glycol(average 10.0 g 10.0 g molecular weight 300) Ethylenediamine tetraaceticacid 4.0 g 4.0 g Sodium sulfite 0.10 g 0.20 g Potassium chloride 10.0 g— Sodium 4,5-dihydroxybenzene- 0.50 g 0.50 g 1,3-disulfonateDisodium-N,N-bis(sulfonatoethyl) 8.5 g 14.0 g hydroxylamine4-amino-3-methyl-N-ethyl-N- 4.8 g 14.0 g(β-methanesulfonamidoethyl)aniline •3/2 sulfate•monohydrate Potassiumcarbonate 26.3 g 26.3 g Water to make 1000 ml 1000 ml pH (25° C.,adjusted using sulfuric 10.15 acid and potassium hydroxide)

(Tank solution) (Replenisher) (Bleach-fixing solution) Water 800 ml 800ml Ammonium thiosulfate (750 g/l) 107 ml 214 ml m-Carboxy benzenesulfinic acid 8.3 g 16.5 g Ammonium iron (III) 47.0 g 94.0 gethylenediaminetetraacetate Ethylenediaminetetraacetic acid 1.4 g 2.8 gNitric acid (67%) 16.5 g 33.0 g Imidazole 14.6 g 29.2 g Ammonium sulfite16.0 g 32.0 g Potassium metabisulfite 23.1 g 46.2 g Water to make 1000ml 1000 ml pH (25° C., adjusted using nitric 6.5 6.5 acid and aqueousammonia) (Rinse solution) Sodium chlorinated-isocyanurate 0.02 g 0.02 gDeionized water 1000 ml 1000 ml (conductivity: 5 μS/cm or less) pH (25°C.) 6.5 6.5

Example 4-4

In the case where the photosensitive materials described in Examples 4-1to 4-3 were exposed to light by the exposure method described below, theeffects of the present invention were exhibited similarly as in Example4-1.

(Method for Exposure)

The scanning exposure was carried out for the photosensitive materialsprepared in Examples 4-1 and 4-2 using a scanning exposure deviceillustrated in FIG. 1 of JP-A-11-88619. As the light source, in thescanning exposure device, a light source of 688 nm (R light) taken outby using a laser semiconductor, a light source of 532 nm (G light) and alight source of 473 nm (B light) each taken out by combining asemiconductor laser with SHG, respectively, were used. The quantity ofeach of lights was modulated by an external modulator, and laser beamswere, in order, scan-exposed to a sample moving in the directionvertical to the scanning direction by the reflection to a rotatingpolyhedron. The scanning pitch was 400 dpi and the average exposure timeper pixel was 8×10⁻⁸ sec. The temperature of the semiconductor laser waskept constant by using a Peltier device to prevent the quantity of lightfrom being changed by temperature.

Example 4-5

Each of the photosensitive materials prepared in Examples 4-1 to 4-4were subjected to scanning exposure by use of the apparatus describedbelow and evaluations according to Examples 4-1 to 4-4 were performed.As a result, it was revealed that the effects of the present invention,that is, use of the samples having the constitution of the presentinvention can give rise to excellent color separability and rapidprocessing suitability, can be obtained significantly.

Digital Minilabo Frontier 330 (trademark, manufactured by Fuji PhotoFilm Co., Ltd.), Lambda 130 (trademark, manufactured by Durst), LIGHTJET5000 (trademark, manufactured by Gretag).

Having described our invention as related to the present embodiments, itis our intention that the invention not be limited by any of the detailsof the description, unless otherwise specified, but rather be construedbroadly within its spirit and scope as set out in the accompanyingclaims.

This nonprovisional application claims priority under 35 U.S.C. § 119(a) on Patent Application No. 2002-56655 filed in Japan on Mar. 1, 2002,Patent Application No. 2002-111023 filed in Japan on Apr. 12, 2002,Patent Application No. 2002-111282 filed in Japan on Apr. 12, 2002, andPatent Application No. 2002-112176 filed in Japan on Apr. 15, 2002,which are herein incorporated by reference.

1. (canceled)
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 9. A silver halide colorphotographic light-sensitive material, having at least one yellowcolor-forming light-sensitive silver halide emulsion layer, at least onemagenta color-forming light-sensitive silver halide emulsion layer, andat least one cyan color-forming light-sensitive silver halide emulsionlayer, on a support, and containing at least one yellow dye-formingcoupler represented by the following formula (I) and at least one cyancoupler represented by the following formula (CC-I):

wherein, in formula (I), Q represents a group of non-metal atomsnecessary to form a 5- to 7-membered ring together with the —N═C—N(R1)-;R1 represents a substituent; R2 represents a substituent; m represents 0to 5; when m is 2 or more, R2s may be the same or different from eachother, or R2s may bond together to form a ring; and X represents ahydrogen atom, or a group capable of being split-off upon a couplingreaction with an oxidized product of a developing agent;

wherein, in formula (CC-I), Ga represents —C(R₂₃)= or —N═; Gb represents—C(R₂₃)=when Ga represents —N═, or Gb represents —N=when Ga represents—C(R₂₃)=; R₂₁ and R₂₂ each independently represent an electronattractive group of which a Hammett's substituent constant σ_(p) valueis 0.20 or more and 1.0 or less; R₂₃ represents a substituent; and Yrepresents a hydrogen atom, or a group capable of being split-off upon acoupling reaction with an oxidized product of a developing agent. 10.The silver halide color photographic light-sensitive material as claimedin claim 9, wherein Q in the formula (I) is a group represented by—C(—R11)=C(—R12)—SO₂— or —C(—R11)=C(—R12)—CO—, in which R11 and R12 bondwith each other to form a 5- to 7-membered ring together with the —C═C—,or R11 and R12 each independently represent a hydrogen atom or asubstituent.
 11. The silver halide color photographic light-sensitivematerial as claimed in claim 9, wherein Q in the formula (I) is a grouprepresented by —C(—R11)=C(—R12)-SO₂—, in which R11 and R12 bond witheach other to form a 5- to 7-membered ring together with the —C═C—, orR11 and R12 each independently represent a hydrogen atom or asubstituent.
 12. The silver halide color photographic light-sensitivematerial as claimed in claim 9, wherein the yellow dye-forming couplerrepresented by formula (I) is a yellow dye-forming coupler representedby formula (II):

wherein, in formula (II), R1 represents a substituent; R2 represents asubstituent; m represents an integer of 0 to 5; when m is 2 or more, R2smay be the same or different from each other, or R2s may bond togetherto form a ring; R3 represents a substituent; n represents an integer of0 to 4; when n is 2 or more, R3s may be the same or different from eachother, or R3s may bond together to form a ring; and X represents ahydrogen atom, or a group capable of being split-off upon a couplingreaction with an oxidized product of a developing agent.
 13. The silverhalide color photographic light-sensitive material as claimed in claim12, wherein R1 in the dye-forming coupler represented by formula (II) isa substituted or unsubstituted alkyl group.
 14. A silver halide colorphotographic light-sensitive material, having at least one yellow colorforming light-sensitive silver halide emulsion layer, at least onemagenta color-forming light-sensitive silver halide emulsion layer, andat least one cyan color-forming light-sensitive silver halide emulsionlayer, on a support, and containing at least one yellow dye-formingcoupler represented by the following formula (I), and at least onecompound selected from the group consisting of compounds represented byany of the following formula [S-I], [S—II], [S-III], [S-IV], [S-V],[S-VI], [ST-I], [ST-II], [ST-III], [ST-IV] or [ST-V] and water-insolublehomopolymers or copolymers:

wherein, in formula (I), Q represents a group of non-metal atomsnecessary to form a 5- to 7-membered ring together with the —N═C—N(R1)-;R1 represents a substituent; R2 represents a substituent; m representsan integer of 0 to 5; when m is 2 or more, R2s may be the same ordifferent from each other, or R2s may bond together to form a ring; andX represents a hydrogen atom, or a group capable of being split-off upona coupling reaction with an oxidized product of a developing agent;

wherein, in formula [S-I], R_(s1), R_(s2) and R_(s3) each independentlyrepresent an alkyl group, a cycloalkyl group, an alkenyl group or anaryl group, in which the total number of carbon atoms contained in thegroups represented by R_(s1), R_(s2) and R_(s3) is 12 to 60;

wherein, in formula [S-II], R_(s4) and R_(s5) each independentlyrepresent an alkyl group, a cycloalkyl group, an alkoxy group or ahalogen atom; s1 represents an integer from 0 to 4; and when s1 is 2 ormore, plural R_(s5)s may be the same or different, and R_(s4) and R_(s5)may bond with each other to form a five- or six-membered ring;R_(s8)-(-COOR_(s7))_(sm)  formula [S-III] wherein, in formula [S-III],R_(s6) represents a linking group having no aromatic group; R_(s7)represents an alkyl, cycloalkyl, alkenyl or alkynyl group having 20 orless carbon atoms; sm represents an integer from 2 or more and 5 orless; and when sm is 2 or more, plural —COOR_(17s) may be the same ordifferent;R_(s8)-(-OCOR_(s9))_(sn)  formula [S-IV] wherein, in formula [S-IV],R_(s8) represents a linking group; R_(s9) represents an alkyl,cycloalkyl, alkenyl or alkynyl group having 20 or less carbon atoms; snrepresents an integer from 2 or more and 5 or less; and when sn is 2 ormore, plural —OCOR_(s9)s may be the same or different;

wherein, in formula [S-V], R_(s10), R_(s11), R_(s12) and R_(s13) eachindependently represent a hydrogen atom, an aliphatic oxycarbonyl groupor a carbamoyl group, in which the total group, an aliphatic oxycarbonylgroup, an aromatic number of carbon atoms contained in R_(s10), R_(s11),R_(s12) and R_(s13) is 8 to 60; and R_(s10) and R_(s11), R_(s10) andR_(s12), or R_(s12) and R_(s13) may bond with each other, to form afive- to seven-membered ring, respectively; with the proviso that all ofR_(s10), R_(s11), R_(s12) and R_(s13) simultaneously do not represent ahydrogen atom;R_(s14)-(-COOR_(s15))_(sp)  formula [S-VI] wherein, in formula [S-VI],R_(s14) represents an aromatic linking group; R_(s15) represents analkyl, cycloalkyl, alkenyl or alkynyl group having 20 or less carbonatoms; sp represents an integer from 3 or more and 5 or less; and whensp is 2 or more, plural —COOR_(s15)s may be

wherein, in formula [ST-I], R₄₀, R₅₀ and R₆₀ each independentlyrepresent an aliphatic group or an aromatic group; and 14, m4 and n4each independently represent 0 or 1, with the proviso that 14, m4 and n4simultaneously are not 1;R_(A)—NH—SO₂—R_(B)  formula [ST-II] wherein, in formula [ST-II], R_(A)and R_(B) each independently represent a hydrogen atom, an alkyl group,a cycloalkyl group, an alkenyl group, a cycloalkenyl group, an alkynylgroup, an aryl group, a heterocyclic group, an alkoxy group, an aryloxygroup, a heterocyclic oxy group, or a group represented by the followingformula:

in which R_(C) and R_(D) each independently represent a hydrogen atom,an alkyl group or an aryl group; and R_(A) and R_(B) each may be thesame or different;

wherein, in formula [ST-III], J′ represents a divalent organic group;and Y represents an alkyl group, a cycloalkyl group, an aryl group, analkenyl group, an alkynyl group, a cycloalkenyl group or a heterocyclicgroup;

wherein, in formula [ST-IV], R₅₁, and R₅₂ each independently representan aliphatic group or —COR₅₃, in which R₅₃ represents an aliphaticgroup; J₅ represents a divalent organic group or simply a connectingbond; and 15 represents an integer from 0 to 6; andR₅₄—Y₅₄  formula [ST-V] wherein, in formula [ST-V], R₅₄ represents ahydrophobic group having the total number of carbon atoms of 10 or more;and Y₅₄ represents a monovalent organic group containing an alcoholichydroxyl group.
 15. The silver halide color photographic light-sensitivematerial as claimed in claim 14, wherein Q in the formula (I) is a grouprepresented by —C(—R11)=C(—R12)-SO₂— or —C(—R11)=C(—R12)-CO—, in whichR11 and R12 bond with each other to form a 5- to 7-membered ringtogether with the —C═C—, or R11 and R12 each independently represent ahydrogen atom or a substituent.
 16. The silver halide color photographiclight-sensitive material as claimed in claim 14, wherein Q in theformula (I) is a group represented by —C(—R11)=C(—R12)—SO₂—, in whichR11 and R12 bond with each other to form a 5- to 7-membered ringtogether with the —C═C—, or R11 and R12 each independently represent ahydrogen atom or a substituent.
 17. The silver halide color photographiclight-sensitive material as claimed in claim 14, wherein the yellowdye-forming coupler represented by formula (I) is a yellow dye-formingcoupler represented by formula (II):

wherein, in formula (II), R1 represents a substituent; R2 represents asubstituent; m represents an integer of 0 to 5; when m is 2 or more, R2smay be the same or different from each other, or R2s may bond togetherto form a ring; R3 represents a substituent; n represents an integer of0 to 4; when n is 2 or more, R3s may be the same or different from eachother, or R3s may bond together to form a ring; and X represents ahydrogen atom, or a group capable of being split-off upon a couplingreaction with an oxidized product of a developing agent.
 18. The silverhalide color photographic light-sensitive material as claimed in claim17, wherein R1 in the dye-forming coupler represented by formula (II) isa substituted or unsubstituted alkyl group.
 19. (canceled) 20.(canceled)
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